Verfügbarkeit: The value of genetic and genomic technologies :

The value of genetic and genomic technologies :: workshop summary /

"Knowing one's genetic disposition to a variety of diseases, including common chronic diseases, can benefit both the individual and society at large. The IOM's Roundtable on Translating Genomic-Based Research for Health held a workshop on March 22, 2010, to bring together diverse pers...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Körperschaft:	Institute of Medicine (U.S.). Roundtable on Translating Genomic-Based Research for Health
Weitere Verfasser:	Wizemann, Theresa M., Berger, Adam C.
Format:	Elektronisch E-Book
Sprache:	English
Veröffentlicht:	Washington, D.C. : National Academies Press, 2010.
Schlagworte:	Genomics > Congresses. Genomics > Research > Congresses. Human chromosome abnormalities > Diagnosis > Congresses. Genetic counseling > Congresses. Genetic disorders > Diagnosis > Congresses. Genetic screening. Medical genetics. Decision making. Genetic counseling. Genetic Testing Genetic Diseases, Inborn > diagnosis Genetic Diseases, Inborn > prevention & control Genetics, Medical Decision Making Genetic Counseling Colorectal Neoplasms, Hereditary Nonpolyposis > genetics Warfarin > therapeutic use Génomique > Congrès. Génomique > Recherche > Congrès. Chromosomes humains > Anomalies > Diagnostic > Congrès. Conseil génétique > Congrès. Maladies génétiques > Diagnostic > Congrès. Dépistage génétique. Génétique médicale. Prise de décision. Conseil génétique. decision making. SCIENCE > Life Sciences > Genetics & Genomics. Medical genetics Genetic screening Decision making Genetic counseling Genetic disorders > Diagnosis Genomics Human chromosome abnormalities > Diagnosis Genetic Predisposition to Disease Genetic Diseases, Inborn diagnosis Electronic books. Conference papers and proceedings
Online-Zugang:	Volltext
Zusammenfassung:	"Knowing one's genetic disposition to a variety of diseases, including common chronic diseases, can benefit both the individual and society at large. The IOM's Roundtable on Translating Genomic-Based Research for Health held a workshop on March 22, 2010, to bring together diverse perspectives on the value of genetic testing, and to discuss its use in clinical practice."--Home page.
Beschreibung:	1 online resource (108 pages)
Bibliographie:	Includes bibliographical references.
ISBN:	9780309157728 0309157722 1282948571 9781282948570

Internformat

MARC


LEADER	00000cam a2200000 a 4500
001	ZDB-4-EBA-ocn672515579
003	OCoLC
005	20241004212047.0
006	m o d
007	cr \|\|\|\|\|\|\|\|\|\|\|
008	101028s2010 dcu ob 100 0 eng d
040			\|a VAM \|b eng \|e pn \|c VAM \|d MMU \|d OCLCQ \|d N$T \|d CDX \|d E7B \|d IDEBK \|d CU3 \|d OCLCQ \|d LCS \|d OCLCQ \|d ORU \|d YDXCP \|d OCLCQ \|d DEBSZ \|d OCLCQ \|d OCLCA \|d NLGGC \|d OCLCO \|d VT2 \|d CUY \|d DKDLA \|d OCLCQ \|d OCLCO \|d EBLCP \|d OCLCO \|d OCLCQ \|d OCLCO \|d OCLCA \|d OCLCQ \|d OCLCO \|d OCLCA \|d TOA \|d OCLCO \|d AGLDB \|d MOR \|d LIP \|d PIFAG \|d MERER \|d ZCU \|d OCLCQ \|d MERUC \|d OCLCQ \|d NJR \|d OCLCO \|d U3W \|d BUF \|d OCLCO \|d KIJ \|d OCLCO \|d OCLCF \|d STF \|d WRM \|d VNS \|d OCLCO \|d OCLCQ \|d VTS \|d COCUF \|d ICG \|d OCLCO \|d OCLCQ \|d WYU \|d LVT \|d TKN \|d DKC \|d AU@ \|d OCLCO \|d OCLCQ \|d M8D \|d OCLCO \|d OCLCQ \|d OCLCO \|d UKAHL \|d OCLCQ \|d K6U \|d OCLCA \|d OCLCO \|d OCLCQ \|d OCL \|d INARC \|d OCLCO \|d OCLCQ \|d OCLCL \|d SFB
019			\|a 703278383 \|a 707822063 \|a 731903300 \|a 755702913 \|a 764548948 \|a 768696299 \|a 772546668 \|a 816630283 \|a 923282214 \|a 961503334 \|a 962571295 \|a 990604387 \|a 1028812692 \|a 1086900296
020			\|a 9780309157728 \|q (electronic bk.)
020			\|a 0309157722 \|q (electronic bk.)
020			\|a 1282948571
020			\|a 9781282948570
020			\|z 0309157714 \|q (pbk.)
020			\|z 9780309157711 \|q (pbk.)
024	8		\|a 9786612948572
035			\|a (OCoLC)672515579 \|z (OCoLC)703278383 \|z (OCoLC)707822063 \|z (OCoLC)731903300 \|z (OCoLC)755702913 \|z (OCoLC)764548948 \|z (OCoLC)768696299 \|z (OCoLC)772546668 \|z (OCoLC)816630283 \|z (OCoLC)923282214 \|z (OCoLC)961503334 \|z (OCoLC)962571295 \|z (OCoLC)990604387 \|z (OCoLC)1028812692 \|z (OCoLC)1086900296
037			\|a 294857 \|b MIL
050		4	\|a QH442 \|b .V8 2010
060		4	\|a 2011 C-397
060		4	\|a QZ 52
072		7	\|a SCI \|x 029000 \|2 bisacsh
072		7	\|a MBGR, MFN \|2 bicssc
082	7		\|a 572.86 \|2 22
049			\|a MAIN
245	0	4	\|a The value of genetic and genomic technologies : \|b workshop summary / \|c Theresa Wizemann and Adam C. Berger, rapporteurs ; Roundtable on Translating Genomic-Based Research for Health ; Board on Health Sciences Policy ; Institute of Medicine of the National Academies.
260			\|a Washington, D.C. : \|b National Academies Press, \|c 2010.
300			\|a 1 online resource (108 pages)
336			\|a text \|b txt \|2 rdacontent
337			\|a computer \|b c \|2 rdamedia
338			\|a online resource \|b cr \|2 rdacarrier
520			\|a "Knowing one's genetic disposition to a variety of diseases, including common chronic diseases, can benefit both the individual and society at large. The IOM's Roundtable on Translating Genomic-Based Research for Health held a workshop on March 22, 2010, to bring together diverse perspectives on the value of genetic testing, and to discuss its use in clinical practice."--Home page.
505	0		\|a Tumor-based screening for Lynch Syndrome -- Pharmacogenomic testing to guide warfarin dosing -- Genomic profiling -- Closing remarks.
504			\|a Includes bibliographical references.
546			\|a English.
650		0	\|a Genomics \|v Congresses.
650		0	\|a Genomics \|x Research \|v Congresses.
650		0	\|a Human chromosome abnormalities \|x Diagnosis \|v Congresses.
650		0	\|a Genetic counseling \|v Congresses.
650		0	\|a Genetic disorders \|x Diagnosis \|v Congresses.
650		0	\|a Genetic screening. \|0 http://id.loc.gov/authorities/subjects/sh99000370
650		0	\|a Medical genetics. \|0 http://id.loc.gov/authorities/subjects/sh85082937
650		0	\|a Decision making. \|0 http://id.loc.gov/authorities/subjects/sh85036199
650		0	\|a Genetic counseling. \|0 http://id.loc.gov/authorities/subjects/sh85053853
650		2	\|a Genetic Testing
650		2	\|a Genetic Diseases, Inborn \|x diagnosis
650		2	\|a Genetic Diseases, Inborn \|x prevention & control
650		2	\|a Genetics, Medical
650		2	\|a Decision Making
650		2	\|a Genetic Counseling
650		2	\|a Colorectal Neoplasms, Hereditary Nonpolyposis \|x genetics
650		2	\|a Warfarin \|x therapeutic use
650		6	\|a Génomique \|v Congrès.
650		6	\|a Génomique \|x Recherche \|v Congrès.
650		6	\|a Chromosomes humains \|x Anomalies \|x Diagnostic \|v Congrès.
650		6	\|a Conseil génétique \|v Congrès.
650		6	\|a Maladies génétiques \|x Diagnostic \|v Congrès.
650		6	\|a Dépistage génétique.
650		6	\|a Génétique médicale.
650		6	\|a Prise de décision.
650		6	\|a Conseil génétique.
650		7	\|a decision making. \|2 aat
650		7	\|a SCIENCE \|x Life Sciences \|x Genetics & Genomics. \|2 bisacsh
650		7	\|a Medical genetics \|2 fast
650		7	\|a Genetic screening \|2 fast
650		7	\|a Decision making \|2 fast
650		7	\|a Genetic counseling \|2 fast
650		7	\|a Genetic disorders \|x Diagnosis \|2 fast
650		7	\|a Genomics \|2 fast
650		7	\|a Human chromosome abnormalities \|x Diagnosis \|2 fast
653			\|a Genetic Testing
653			\|a Genomics
653			\|a Genetic Predisposition to Disease
653			\|a Genetic Diseases, Inborn diagnosis
655		0	\|a Electronic books.
655		7	\|a Conference papers and proceedings \|2 fast
700	1		\|a Wizemann, Theresa M.
700	1		\|a Berger, Adam C. \|0 http://id.loc.gov/authorities/names/no2010177254
710	2		\|a Institute of Medicine (U.S.). \|b Roundtable on Translating Genomic-Based Research for Health. \|0 http://id.loc.gov/authorities/names/no2008119550
758			\|i has work: \|a The value of genetic and genomic technologies (Text) \|1 https://id.oclc.org/worldcat/entity/E39PCH3MkbH4cc8wBWD3PPg9pd \|4 https://id.oclc.org/worldcat/ontology/hasWork
776	0	8	\|i Print version: \|d Washington, D.C. : National Academies Press, 2010 \|z 0309157714 \|z 9780309157711 \|w (OCoLC)668941930
856	4	0	\|l FWS01 \|p ZDB-4-EBA \|q FWS_PDA_EBA \|u https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=350891 \|3 Volltext
938			\|a Internet Archive \|b INAR \|n valueofgeneticge0000unse
938			\|a Askews and Holts Library Services \|b ASKH \|n AH36617229
938			\|a Askews and Holts Library Services \|b ASKH \|n AH36559422
938			\|a Coutts Information Services \|b COUT \|n 17157557
938			\|a ProQuest Ebook Central \|b EBLB \|n EBL3378716
938			\|a ebrary \|b EBRY \|n ebr10439396
938			\|a EBSCOhost \|b EBSC \|n 350891
938			\|a ProQuest MyiLibrary Digital eBook Collection \|b IDEB \|n 294857
938			\|a YBP Library Services \|b YANK \|n 3635987
994			\|a 92 \|b GEBAY
912			\|a ZDB-4-EBA
049			\|a DE-863

Datensatz im Suchindex

DE-BY-FWS_katkey	ZDB-4-EBA-ocn672515579
_version_	1816881743945269248
adam_text
any_adam_object
author2	Wizemann, Theresa M. Berger, Adam C.
author2_role
author2_variant	t m w tm tmw a c b ac acb
author_GND	http://id.loc.gov/authorities/names/no2010177254
author_corporate	Institute of Medicine (U.S.). Roundtable on Translating Genomic-Based Research for Health
author_corporate_role
author_facet	Wizemann, Theresa M. Berger, Adam C. Institute of Medicine (U.S.). Roundtable on Translating Genomic-Based Research for Health
author_sort	Wizemann, Theresa M.
building	Verbundindex
bvnumber	localFWS
callnumber-first	Q - Science
callnumber-label	QH442
callnumber-raw	QH442 .V8 2010
callnumber-search	QH442 .V8 2010
callnumber-sort	QH 3442 V8 42010
callnumber-subject	QH - Natural History and Biology
collection	ZDB-4-EBA
contents	Tumor-based screening for Lynch Syndrome -- Pharmacogenomic testing to guide warfarin dosing -- Genomic profiling -- Closing remarks.
ctrlnum	(OCoLC)672515579
dewey-full	572.86
dewey-hundreds	500 - Natural sciences and mathematics
dewey-ones	572 - Biochemistry
dewey-raw	572.86
dewey-search	572.86
dewey-sort	3572.86
dewey-tens	570 - Biology
discipline	Biologie
format	Electronic eBook
fullrecord	<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>06160cam a2201117 a 4500</leader><controlfield tag="001">ZDB-4-EBA-ocn672515579</controlfield><controlfield tag="003">OCoLC</controlfield><controlfield tag="005">20241004212047.0</controlfield><controlfield tag="006">m o d </controlfield><controlfield tag="007">cr \|\|\|\|\|\|\|\|\|\|\|</controlfield><controlfield tag="008">101028s2010 dcu ob 100 0 eng d</controlfield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">VAM</subfield><subfield code="b">eng</subfield><subfield code="e">pn</subfield><subfield code="c">VAM</subfield><subfield code="d">MMU</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">N$T</subfield><subfield code="d">CDX</subfield><subfield code="d">E7B</subfield><subfield code="d">IDEBK</subfield><subfield code="d">CU3</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">LCS</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">ORU</subfield><subfield code="d">YDXCP</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">DEBSZ</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">OCLCA</subfield><subfield code="d">NLGGC</subfield><subfield code="d">OCLCO</subfield><subfield code="d">VT2</subfield><subfield code="d">CUY</subfield><subfield code="d">DKDLA</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">OCLCO</subfield><subfield code="d">EBLCP</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCA</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCA</subfield><subfield code="d">TOA</subfield><subfield code="d">OCLCO</subfield><subfield code="d">AGLDB</subfield><subfield code="d">MOR</subfield><subfield code="d">LIP</subfield><subfield code="d">PIFAG</subfield><subfield code="d">MERER</subfield><subfield code="d">ZCU</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">MERUC</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">NJR</subfield><subfield code="d">OCLCO</subfield><subfield code="d">U3W</subfield><subfield code="d">BUF</subfield><subfield code="d">OCLCO</subfield><subfield code="d">KIJ</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCF</subfield><subfield code="d">STF</subfield><subfield code="d">WRM</subfield><subfield code="d">VNS</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">VTS</subfield><subfield code="d">COCUF</subfield><subfield code="d">ICG</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">WYU</subfield><subfield code="d">LVT</subfield><subfield code="d">TKN</subfield><subfield code="d">DKC</subfield><subfield code="d">AU@</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">M8D</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">OCLCO</subfield><subfield code="d">UKAHL</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">K6U</subfield><subfield code="d">OCLCA</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">OCL</subfield><subfield code="d">INARC</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">OCLCL</subfield><subfield code="d">SFB</subfield></datafield><datafield tag="019" ind1=" " ind2=" "><subfield code="a">703278383</subfield><subfield code="a">707822063</subfield><subfield code="a">731903300</subfield><subfield code="a">755702913</subfield><subfield code="a">764548948</subfield><subfield code="a">768696299</subfield><subfield code="a">772546668</subfield><subfield code="a">816630283</subfield><subfield code="a">923282214</subfield><subfield code="a">961503334</subfield><subfield code="a">962571295</subfield><subfield code="a">990604387</subfield><subfield code="a">1028812692</subfield><subfield code="a">1086900296</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9780309157728</subfield><subfield code="q">(electronic bk.)</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">0309157722</subfield><subfield code="q">(electronic bk.)</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">1282948571</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9781282948570</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="z">0309157714</subfield><subfield code="q">(pbk.)</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="z">9780309157711</subfield><subfield code="q">(pbk.)</subfield></datafield><datafield tag="024" ind1="8" ind2=" "><subfield code="a">9786612948572</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)672515579</subfield><subfield code="z">(OCoLC)703278383</subfield><subfield code="z">(OCoLC)707822063</subfield><subfield code="z">(OCoLC)731903300</subfield><subfield code="z">(OCoLC)755702913</subfield><subfield code="z">(OCoLC)764548948</subfield><subfield code="z">(OCoLC)768696299</subfield><subfield code="z">(OCoLC)772546668</subfield><subfield code="z">(OCoLC)816630283</subfield><subfield code="z">(OCoLC)923282214</subfield><subfield code="z">(OCoLC)961503334</subfield><subfield code="z">(OCoLC)962571295</subfield><subfield code="z">(OCoLC)990604387</subfield><subfield code="z">(OCoLC)1028812692</subfield><subfield code="z">(OCoLC)1086900296</subfield></datafield><datafield tag="037" ind1=" " ind2=" "><subfield code="a">294857</subfield><subfield code="b">MIL</subfield></datafield><datafield tag="050" ind1=" " ind2="4"><subfield code="a">QH442</subfield><subfield code="b">.V8 2010</subfield></datafield><datafield tag="060" ind1=" " ind2="4"><subfield code="a">2011 C-397</subfield></datafield><datafield tag="060" ind1=" " ind2="4"><subfield code="a">QZ 52</subfield></datafield><datafield tag="072" ind1=" " ind2="7"><subfield code="a">SCI</subfield><subfield code="x">029000</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="072" ind1=" " ind2="7"><subfield code="a">MBGR, MFN</subfield><subfield code="2">bicssc</subfield></datafield><datafield tag="082" ind1="7" ind2=" "><subfield code="a">572.86</subfield><subfield code="2">22</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">MAIN</subfield></datafield><datafield tag="245" ind1="0" ind2="4"><subfield code="a">The value of genetic and genomic technologies :</subfield><subfield code="b">workshop summary /</subfield><subfield code="c">Theresa Wizemann and Adam C. Berger, rapporteurs ; Roundtable on Translating Genomic-Based Research for Health ; Board on Health Sciences Policy ; Institute of Medicine of the National Academies.</subfield></datafield><datafield tag="260" ind1=" " ind2=" "><subfield code="a">Washington, D.C. :</subfield><subfield code="b">National Academies Press,</subfield><subfield code="c">2010.</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 online resource (108 pages)</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">computer</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">online resource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">"Knowing one's genetic disposition to a variety of diseases, including common chronic diseases, can benefit both the individual and society at large. The IOM's Roundtable on Translating Genomic-Based Research for Health held a workshop on March 22, 2010, to bring together diverse perspectives on the value of genetic testing, and to discuss its use in clinical practice."--Home page.</subfield></datafield><datafield tag="505" ind1="0" ind2=" "><subfield code="a">Tumor-based screening for Lynch Syndrome -- Pharmacogenomic testing to guide warfarin dosing -- Genomic profiling -- Closing remarks.</subfield></datafield><datafield tag="504" ind1=" " ind2=" "><subfield code="a">Includes bibliographical references.</subfield></datafield><datafield tag="546" ind1=" " ind2=" "><subfield code="a">English.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Genomics</subfield><subfield code="v">Congresses.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Genomics</subfield><subfield code="x">Research</subfield><subfield code="v">Congresses.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Human chromosome abnormalities</subfield><subfield code="x">Diagnosis</subfield><subfield code="v">Congresses.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Genetic counseling</subfield><subfield code="v">Congresses.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Genetic disorders</subfield><subfield code="x">Diagnosis</subfield><subfield code="v">Congresses.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Genetic screening.</subfield><subfield code="0">http://id.loc.gov/authorities/subjects/sh99000370</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Medical genetics.</subfield><subfield code="0">http://id.loc.gov/authorities/subjects/sh85082937</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Decision making.</subfield><subfield code="0">http://id.loc.gov/authorities/subjects/sh85036199</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Genetic counseling.</subfield><subfield code="0">http://id.loc.gov/authorities/subjects/sh85053853</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">Genetic Testing</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">Genetic Diseases, Inborn</subfield><subfield code="x">diagnosis</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">Genetic Diseases, Inborn</subfield><subfield code="x">prevention & control</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">Genetics, Medical</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">Decision Making</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">Genetic Counseling</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">Colorectal Neoplasms, Hereditary Nonpolyposis</subfield><subfield code="x">genetics</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">Warfarin</subfield><subfield code="x">therapeutic use</subfield></datafield><datafield tag="650" ind1=" " ind2="6"><subfield code="a">Génomique</subfield><subfield code="v">Congrès.</subfield></datafield><datafield tag="650" ind1=" " ind2="6"><subfield code="a">Génomique</subfield><subfield code="x">Recherche</subfield><subfield code="v">Congrès.</subfield></datafield><datafield tag="650" ind1=" " ind2="6"><subfield code="a">Chromosomes humains</subfield><subfield code="x">Anomalies</subfield><subfield code="x">Diagnostic</subfield><subfield code="v">Congrès.</subfield></datafield><datafield tag="650" ind1=" " ind2="6"><subfield code="a">Conseil génétique</subfield><subfield code="v">Congrès.</subfield></datafield><datafield tag="650" ind1=" " ind2="6"><subfield code="a">Maladies génétiques</subfield><subfield code="x">Diagnostic</subfield><subfield code="v">Congrès.</subfield></datafield><datafield tag="650" ind1=" " ind2="6"><subfield code="a">Dépistage génétique.</subfield></datafield><datafield tag="650" ind1=" " ind2="6"><subfield code="a">Génétique médicale.</subfield></datafield><datafield tag="650" ind1=" " ind2="6"><subfield code="a">Prise de décision.</subfield></datafield><datafield tag="650" ind1=" " ind2="6"><subfield code="a">Conseil génétique.</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">decision making.</subfield><subfield code="2">aat</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">SCIENCE</subfield><subfield code="x">Life Sciences</subfield><subfield code="x">Genetics & Genomics.</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Medical genetics</subfield><subfield code="2">fast</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Genetic screening</subfield><subfield code="2">fast</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Decision making</subfield><subfield code="2">fast</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Genetic counseling</subfield><subfield code="2">fast</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Genetic disorders</subfield><subfield code="x">Diagnosis</subfield><subfield code="2">fast</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Genomics</subfield><subfield code="2">fast</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Human chromosome abnormalities</subfield><subfield code="x">Diagnosis</subfield><subfield code="2">fast</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Genetic Testing</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Genomics</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Genetic Predisposition to Disease</subfield></datafield><datafield tag="653" ind1=" " ind2=" "><subfield code="a">Genetic Diseases, Inborn diagnosis</subfield></datafield><datafield tag="655" ind1=" " ind2="0"><subfield code="a">Electronic books.</subfield></datafield><datafield tag="655" ind1=" " ind2="7"><subfield code="a">Conference papers and proceedings</subfield><subfield code="2">fast</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Wizemann, Theresa M.</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Berger, Adam C.</subfield><subfield code="0">http://id.loc.gov/authorities/names/no2010177254</subfield></datafield><datafield tag="710" ind1="2" ind2=" "><subfield code="a">Institute of Medicine (U.S.).</subfield><subfield code="b">Roundtable on Translating Genomic-Based Research for Health.</subfield><subfield code="0">http://id.loc.gov/authorities/names/no2008119550</subfield></datafield><datafield tag="758" ind1=" " ind2=" "><subfield code="i">has work:</subfield><subfield code="a">The value of genetic and genomic technologies (Text)</subfield><subfield code="1">https://id.oclc.org/worldcat/entity/E39PCH3MkbH4cc8wBWD3PPg9pd</subfield><subfield code="4">https://id.oclc.org/worldcat/ontology/hasWork</subfield></datafield><datafield tag="776" ind1="0" ind2="8"><subfield code="i">Print version:</subfield><subfield code="d">Washington, D.C. : National Academies Press, 2010</subfield><subfield code="z">0309157714</subfield><subfield code="z">9780309157711</subfield><subfield code="w">(OCoLC)668941930</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="l">FWS01</subfield><subfield code="p">ZDB-4-EBA</subfield><subfield code="q">FWS_PDA_EBA</subfield><subfield code="u">https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=350891</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">Internet Archive</subfield><subfield code="b">INAR</subfield><subfield code="n">valueofgeneticge0000unse</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">Askews and Holts Library Services</subfield><subfield code="b">ASKH</subfield><subfield code="n">AH36617229</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">Askews and Holts Library Services</subfield><subfield code="b">ASKH</subfield><subfield code="n">AH36559422</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">Coutts Information Services</subfield><subfield code="b">COUT</subfield><subfield code="n">17157557</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">ProQuest Ebook Central</subfield><subfield code="b">EBLB</subfield><subfield code="n">EBL3378716</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">ebrary</subfield><subfield code="b">EBRY</subfield><subfield code="n">ebr10439396</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">EBSCOhost</subfield><subfield code="b">EBSC</subfield><subfield code="n">350891</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">ProQuest MyiLibrary Digital eBook Collection</subfield><subfield code="b">IDEB</subfield><subfield code="n">294857</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">YBP Library Services</subfield><subfield code="b">YANK</subfield><subfield code="n">3635987</subfield></datafield><datafield tag="994" ind1=" " ind2=" "><subfield code="a">92</subfield><subfield code="b">GEBAY</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-4-EBA</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">DE-863</subfield></datafield></record></collection>
genre	Electronic books. Conference papers and proceedings fast
genre_facet	Electronic books. Conference papers and proceedings
id	ZDB-4-EBA-ocn672515579
illustrated	Not Illustrated
indexdate	2024-11-27T13:17:35Z
institution	BVB
institution_GND	http://id.loc.gov/authorities/names/no2008119550
isbn	9780309157728 0309157722 1282948571 9781282948570
language	English
oclc_num	672515579
open_access_boolean
owner	MAIN DE-863 DE-BY-FWS
owner_facet	MAIN DE-863 DE-BY-FWS
physical	1 online resource (108 pages)
psigel	ZDB-4-EBA
publishDate	2010
publishDateSearch	2010
publishDateSort	2010
publisher	National Academies Press,
record_format	marc
spelling	The value of genetic and genomic technologies : workshop summary / Theresa Wizemann and Adam C. Berger, rapporteurs ; Roundtable on Translating Genomic-Based Research for Health ; Board on Health Sciences Policy ; Institute of Medicine of the National Academies. Washington, D.C. : National Academies Press, 2010. 1 online resource (108 pages) text txt rdacontent computer c rdamedia online resource cr rdacarrier "Knowing one's genetic disposition to a variety of diseases, including common chronic diseases, can benefit both the individual and society at large. The IOM's Roundtable on Translating Genomic-Based Research for Health held a workshop on March 22, 2010, to bring together diverse perspectives on the value of genetic testing, and to discuss its use in clinical practice."--Home page. Tumor-based screening for Lynch Syndrome -- Pharmacogenomic testing to guide warfarin dosing -- Genomic profiling -- Closing remarks. Includes bibliographical references. English. Genomics Congresses. Genomics Research Congresses. Human chromosome abnormalities Diagnosis Congresses. Genetic counseling Congresses. Genetic disorders Diagnosis Congresses. Genetic screening. http://id.loc.gov/authorities/subjects/sh99000370 Medical genetics. http://id.loc.gov/authorities/subjects/sh85082937 Decision making. http://id.loc.gov/authorities/subjects/sh85036199 Genetic counseling. http://id.loc.gov/authorities/subjects/sh85053853 Genetic Testing Genetic Diseases, Inborn diagnosis Genetic Diseases, Inborn prevention & control Genetics, Medical Decision Making Genetic Counseling Colorectal Neoplasms, Hereditary Nonpolyposis genetics Warfarin therapeutic use Génomique Congrès. Génomique Recherche Congrès. Chromosomes humains Anomalies Diagnostic Congrès. Conseil génétique Congrès. Maladies génétiques Diagnostic Congrès. Dépistage génétique. Génétique médicale. Prise de décision. Conseil génétique. decision making. aat SCIENCE Life Sciences Genetics & Genomics. bisacsh Medical genetics fast Genetic screening fast Decision making fast Genetic counseling fast Genetic disorders Diagnosis fast Genomics fast Human chromosome abnormalities Diagnosis fast Genomics Genetic Predisposition to Disease Electronic books. Conference papers and proceedings fast Wizemann, Theresa M. Berger, Adam C. http://id.loc.gov/authorities/names/no2010177254 Institute of Medicine (U.S.). Roundtable on Translating Genomic-Based Research for Health. http://id.loc.gov/authorities/names/no2008119550 has work: The value of genetic and genomic technologies (Text) https://id.oclc.org/worldcat/entity/E39PCH3MkbH4cc8wBWD3PPg9pd https://id.oclc.org/worldcat/ontology/hasWork Print version: Washington, D.C. : National Academies Press, 2010 0309157714 9780309157711 (OCoLC)668941930 FWS01 ZDB-4-EBA FWS_PDA_EBA https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=350891 Volltext
spellingShingle	The value of genetic and genomic technologies : workshop summary / Tumor-based screening for Lynch Syndrome -- Pharmacogenomic testing to guide warfarin dosing -- Genomic profiling -- Closing remarks. Genomics Congresses. Genomics Research Congresses. Human chromosome abnormalities Diagnosis Congresses. Genetic counseling Congresses. Genetic disorders Diagnosis Congresses. Genetic screening. http://id.loc.gov/authorities/subjects/sh99000370 Medical genetics. http://id.loc.gov/authorities/subjects/sh85082937 Decision making. http://id.loc.gov/authorities/subjects/sh85036199 Genetic counseling. http://id.loc.gov/authorities/subjects/sh85053853 Genetic Testing Genetic Diseases, Inborn diagnosis Genetic Diseases, Inborn prevention & control Genetics, Medical Decision Making Genetic Counseling Colorectal Neoplasms, Hereditary Nonpolyposis genetics Warfarin therapeutic use Génomique Congrès. Génomique Recherche Congrès. Chromosomes humains Anomalies Diagnostic Congrès. Conseil génétique Congrès. Maladies génétiques Diagnostic Congrès. Dépistage génétique. Génétique médicale. Prise de décision. Conseil génétique. decision making. aat SCIENCE Life Sciences Genetics & Genomics. bisacsh Medical genetics fast Genetic screening fast Decision making fast Genetic counseling fast Genetic disorders Diagnosis fast Genomics fast Human chromosome abnormalities Diagnosis fast
subject_GND	http://id.loc.gov/authorities/subjects/sh99000370 http://id.loc.gov/authorities/subjects/sh85082937 http://id.loc.gov/authorities/subjects/sh85036199 http://id.loc.gov/authorities/subjects/sh85053853
title	The value of genetic and genomic technologies : workshop summary /
title_auth	The value of genetic and genomic technologies : workshop summary /
title_exact_search	The value of genetic and genomic technologies : workshop summary /
title_full	The value of genetic and genomic technologies : workshop summary / Theresa Wizemann and Adam C. Berger, rapporteurs ; Roundtable on Translating Genomic-Based Research for Health ; Board on Health Sciences Policy ; Institute of Medicine of the National Academies.
title_fullStr	The value of genetic and genomic technologies : workshop summary / Theresa Wizemann and Adam C. Berger, rapporteurs ; Roundtable on Translating Genomic-Based Research for Health ; Board on Health Sciences Policy ; Institute of Medicine of the National Academies.
title_full_unstemmed	The value of genetic and genomic technologies : workshop summary / Theresa Wizemann and Adam C. Berger, rapporteurs ; Roundtable on Translating Genomic-Based Research for Health ; Board on Health Sciences Policy ; Institute of Medicine of the National Academies.
title_short	The value of genetic and genomic technologies :
title_sort	value of genetic and genomic technologies workshop summary
title_sub	workshop summary /
topic	Genomics Congresses. Genomics Research Congresses. Human chromosome abnormalities Diagnosis Congresses. Genetic counseling Congresses. Genetic disorders Diagnosis Congresses. Genetic screening. http://id.loc.gov/authorities/subjects/sh99000370 Medical genetics. http://id.loc.gov/authorities/subjects/sh85082937 Decision making. http://id.loc.gov/authorities/subjects/sh85036199 Genetic counseling. http://id.loc.gov/authorities/subjects/sh85053853 Genetic Testing Genetic Diseases, Inborn diagnosis Genetic Diseases, Inborn prevention & control Genetics, Medical Decision Making Genetic Counseling Colorectal Neoplasms, Hereditary Nonpolyposis genetics Warfarin therapeutic use Génomique Congrès. Génomique Recherche Congrès. Chromosomes humains Anomalies Diagnostic Congrès. Conseil génétique Congrès. Maladies génétiques Diagnostic Congrès. Dépistage génétique. Génétique médicale. Prise de décision. Conseil génétique. decision making. aat SCIENCE Life Sciences Genetics & Genomics. bisacsh Medical genetics fast Genetic screening fast Decision making fast Genetic counseling fast Genetic disorders Diagnosis fast Genomics fast Human chromosome abnormalities Diagnosis fast
topic_facet	Genomics Congresses. Genomics Research Congresses. Human chromosome abnormalities Diagnosis Congresses. Genetic counseling Congresses. Genetic disorders Diagnosis Congresses. Genetic screening. Medical genetics. Decision making. Genetic counseling. Genetic Testing Genetic Diseases, Inborn diagnosis Genetic Diseases, Inborn prevention & control Genetics, Medical Decision Making Genetic Counseling Colorectal Neoplasms, Hereditary Nonpolyposis genetics Warfarin therapeutic use Génomique Congrès. Génomique Recherche Congrès. Chromosomes humains Anomalies Diagnostic Congrès. Conseil génétique Congrès. Maladies génétiques Diagnostic Congrès. Dépistage génétique. Génétique médicale. Prise de décision. Conseil génétique. decision making. SCIENCE Life Sciences Genetics & Genomics. Medical genetics Genetic screening Decision making Genetic counseling Genetic disorders Diagnosis Genomics Human chromosome abnormalities Diagnosis Electronic books. Conference papers and proceedings
url	https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=350891
work_keys_str_mv	AT wizemanntheresam thevalueofgeneticandgenomictechnologiesworkshopsummary AT bergeradamc thevalueofgeneticandgenomictechnologiesworkshopsummary AT instituteofmedicineusroundtableontranslatinggenomicbasedresearchforhealth thevalueofgeneticandgenomictechnologiesworkshopsummary AT wizemanntheresam valueofgeneticandgenomictechnologiesworkshopsummary AT bergeradamc valueofgeneticandgenomictechnologiesworkshopsummary AT instituteofmedicineusroundtableontranslatinggenomicbasedresearchforhealth valueofgeneticandgenomictechnologiesworkshopsummary

Verfügbarkeit

Es ist kein Print-Exemplar vorhanden.

Volltext öffnen

MARC

Datensatz im Suchindex

Es ist kein Print-Exemplar vorhanden.

Ähnliche Einträge