Neurogenetic developmental disorders: variation of manifestation in childhood
Gespeichert in:
Format: | Elektronisch E-Book |
---|---|
Sprache: | English |
Veröffentlicht: |
Cambridge, Mass.
MIT Press
c2007
|
Schriftenreihe: | Issues in clinical and cognitive neuropsychology
|
Schlagworte: | |
Online-Zugang: | FAW01 FAW02 Volltext |
Beschreibung: | Includes bibliographical references and index Turner syndrome in childhood - Marsha L. Davenport, Stephen R. Hooper and Martha Zeger -- - Klinefelter syndrome - Judith L. Ross, Gerry A. Stefanatos and David Roeltgen -- - Fragile X syndrome : the journey from genes to behavior - Kimberly M. Cornish, Andrew Levitas and Vicki Sudhalter -- - Duchenne muscular dystrophy - Veronica J. Hinton and Edward M. Goldstein -- - Neurofibromatosis - John M. Slopis and Bartlett D. Moore III -- - Cognitive and behavioral characteristics of children with chromosome 22q11.2 deletion syndrome - Tony J. Simon, Merav Burg-Malki and Doron Gothelf -- - Williams Syndrome - Carolyn B. Mervis and Colleen A. Morris -- - Congenital hypothyroidism : genetic and biochemical influences on brain development and neuropsychological functioning - Joanne F. Rovet and Rosalind Brown -- - Inborn errors of metabolism - Kevin M. Antshel and Georgianne Arnold -- - Neurodevelopmental effects of childhood exposure to heavy metals : lessons from pediatric lead poisoning - Theodore I. Lidsky, Agnes T. Heaney, Jay S. Schneider and John F. Rosen -- - Beyond the diagnosis : the process of genetic counseling - Allyn McConkie-Rosell and Julianne O'Daniel -- - From diagnosis to adaptation : optimizing family and child functioning when a genetic diagnosis is associated with mental retardation - Laraine Masters Glidden and Sarah A. Schoolcraft -- - When a genetic disorder is associated with learning disabilities - Michele M. M. Mazzocco -- - Early intervention and early childhood special education for young children with neurogenetic disorders - Deborah D. Hatton -- - The individualized education program : navigating the IEP development process - Vicki Sudhalter |
Beschreibung: | 1 Online-Ressource (xiv, 507 p.) |
ISBN: | 0262134802 0262279320 1429477156 9780262134804 9780262279321 9781429477154 |
Internformat
MARC
LEADER | 00000nmm a2200000zc 4500 | ||
---|---|---|---|
001 | BV043122069 | ||
003 | DE-604 | ||
005 | 00000000000000.0 | ||
007 | cr|uuu---uuuuu | ||
008 | 151126s2007 |||| o||u| ||||||eng d | ||
020 | |a 0262134802 |c hc : alk. paper |9 0-262-13480-2 | ||
020 | |a 0262279320 |c electronic bk. |9 0-262-27932-0 | ||
020 | |a 1429477156 |c electronic bk. |9 1-4294-7715-6 | ||
020 | |a 9780262134804 |c hc : alk. paper |9 978-0-262-13480-4 | ||
020 | |a 9780262279321 |c electronic bk. |9 978-0-262-27932-1 | ||
020 | |a 9781429477154 |c electronic bk. |9 978-1-4294-7715-4 | ||
035 | |a (OCoLC)144569767 | ||
035 | |a (DE-599)BVBBV043122069 | ||
040 | |a DE-604 |b ger |e aacr | ||
041 | 0 | |a eng | |
049 | |a DE-1046 |a DE-1047 | ||
082 | 0 | |a 618.92/8588 |2 22 | |
245 | 1 | 0 | |a Neurogenetic developmental disorders |b variation of manifestation in childhood |c edited by Michèle M.M. Mazzocco and Judith L. Ross |
264 | 1 | |a Cambridge, Mass. |b MIT Press |c c2007 | |
300 | |a 1 Online-Ressource (xiv, 507 p.) | ||
336 | |b txt |2 rdacontent | ||
337 | |b c |2 rdamedia | ||
338 | |b cr |2 rdacarrier | ||
490 | 0 | |a Issues in clinical and cognitive neuropsychology | |
500 | |a Includes bibliographical references and index | ||
500 | |a Turner syndrome in childhood - Marsha L. Davenport, Stephen R. Hooper and Martha Zeger -- - Klinefelter syndrome - Judith L. Ross, Gerry A. Stefanatos and David Roeltgen -- - Fragile X syndrome : the journey from genes to behavior - Kimberly M. Cornish, Andrew Levitas and Vicki Sudhalter -- - Duchenne muscular dystrophy - Veronica J. Hinton and Edward M. Goldstein -- - Neurofibromatosis - John M. Slopis and Bartlett D. Moore III -- - Cognitive and behavioral characteristics of children with chromosome 22q11.2 deletion syndrome - Tony J. Simon, Merav Burg-Malki and Doron Gothelf -- - Williams Syndrome - Carolyn B. Mervis and Colleen A. Morris -- - Congenital hypothyroidism : genetic and biochemical influences on brain development and neuropsychological functioning - Joanne F. Rovet and Rosalind Brown -- - Inborn errors of metabolism - Kevin M. Antshel and Georgianne Arnold -- - Neurodevelopmental effects of childhood exposure to heavy metals : lessons from pediatric lead poisoning - Theodore I. Lidsky, Agnes T. Heaney, Jay S. Schneider and John F. Rosen -- - Beyond the diagnosis : the process of genetic counseling - Allyn McConkie-Rosell and Julianne O'Daniel -- - From diagnosis to adaptation : optimizing family and child functioning when a genetic diagnosis is associated with mental retardation - Laraine Masters Glidden and Sarah A. Schoolcraft -- - When a genetic disorder is associated with learning disabilities - Michele M. M. Mazzocco -- - Early intervention and early childhood special education for young children with neurogenetic disorders - Deborah D. Hatton -- - The individualized education program : navigating the IEP development process - Vicki Sudhalter | ||
650 | 7 | |a Chromosome abnormalities |2 fast | |
650 | 7 | |a Developmental disabilities / Genetic aspects |2 fast | |
650 | 7 | |a Neurogenetics |2 fast | |
650 | 7 | |a Pediatric neuropsychology |2 fast | |
650 | 4 | |a Genetic Diseases, Inborn / diagnosis | |
650 | 4 | |a Child | |
650 | 4 | |a Genetic Counseling / methods | |
650 | 4 | |a Heredodegenerative Disorders, Nervous System / diagnosis | |
650 | 4 | |a Sex Chromosome Disorders / diagnosis | |
650 | 4 | |a Developmental disabilities |x Genetic aspects | |
650 | 4 | |a Chromosome abnormalities | |
650 | 4 | |a Neurogenetics | |
650 | 4 | |a Pediatric neuropsychology | |
650 | 0 | 7 | |a Neurogenetik |0 (DE-588)4589213-1 |2 gnd |9 rswk-swf |
650 | 0 | 7 | |a Entwicklungsstörung |0 (DE-588)4014966-3 |2 gnd |9 rswk-swf |
655 | 7 | |8 1\p |0 (DE-588)4143413-4 |a Aufsatzsammlung |2 gnd-content | |
689 | 0 | 0 | |a Entwicklungsstörung |0 (DE-588)4014966-3 |D s |
689 | 0 | 1 | |a Neurogenetik |0 (DE-588)4589213-1 |D s |
689 | 0 | |8 2\p |5 DE-604 | |
700 | 1 | |a Mazzocco, Michèle M. M. |e Sonstige |4 oth | |
700 | 1 | |a Ross, Judith L. |e Sonstige |4 oth | |
856 | 4 | 0 | |u http://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&db=nlabk&AN=190978 |x Aggregator |3 Volltext |
912 | |a ZDB-4-EBA | ||
999 | |a oai:aleph.bib-bvb.de:BVB01-028546260 | ||
883 | 1 | |8 1\p |a cgwrk |d 20201028 |q DE-101 |u https://d-nb.info/provenance/plan#cgwrk | |
883 | 1 | |8 2\p |a cgwrk |d 20201028 |q DE-101 |u https://d-nb.info/provenance/plan#cgwrk | |
966 | e | |u http://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&db=nlabk&AN=190978 |l FAW01 |p ZDB-4-EBA |q FAW_PDA_EBA |x Aggregator |3 Volltext | |
966 | e | |u http://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&db=nlabk&AN=190978 |l FAW02 |p ZDB-4-EBA |q FAW_PDA_EBA |x Aggregator |3 Volltext |
Datensatz im Suchindex
_version_ | 1804175552484999168 |
---|---|
any_adam_object | |
building | Verbundindex |
bvnumber | BV043122069 |
collection | ZDB-4-EBA |
ctrlnum | (OCoLC)144569767 (DE-599)BVBBV043122069 |
dewey-full | 618.92/8588 |
dewey-hundreds | 600 - Technology (Applied sciences) |
dewey-ones | 618 - Gynecology, obstetrics, pediatrics, geriatrics |
dewey-raw | 618.92/8588 |
dewey-search | 618.92/8588 |
dewey-sort | 3618.92 48588 |
dewey-tens | 610 - Medicine and health |
discipline | Medizin |
format | Electronic eBook |
fullrecord | <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>04671nmm a2200673zc 4500</leader><controlfield tag="001">BV043122069</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">00000000000000.0</controlfield><controlfield tag="007">cr|uuu---uuuuu</controlfield><controlfield tag="008">151126s2007 |||| o||u| ||||||eng d</controlfield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">0262134802</subfield><subfield code="c">hc : alk. paper</subfield><subfield code="9">0-262-13480-2</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">0262279320</subfield><subfield code="c">electronic bk.</subfield><subfield code="9">0-262-27932-0</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">1429477156</subfield><subfield code="c">electronic bk.</subfield><subfield code="9">1-4294-7715-6</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9780262134804</subfield><subfield code="c">hc : alk. paper</subfield><subfield code="9">978-0-262-13480-4</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9780262279321</subfield><subfield code="c">electronic bk.</subfield><subfield code="9">978-0-262-27932-1</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9781429477154</subfield><subfield code="c">electronic bk.</subfield><subfield code="9">978-1-4294-7715-4</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)144569767</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)BVBBV043122069</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-604</subfield><subfield code="b">ger</subfield><subfield code="e">aacr</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">DE-1046</subfield><subfield code="a">DE-1047</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">618.92/8588</subfield><subfield code="2">22</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Neurogenetic developmental disorders</subfield><subfield code="b">variation of manifestation in childhood</subfield><subfield code="c">edited by Michèle M.M. Mazzocco and Judith L. Ross</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Cambridge, Mass.</subfield><subfield code="b">MIT Press</subfield><subfield code="c">c2007</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 Online-Ressource (xiv, 507 p.)</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="490" ind1="0" ind2=" "><subfield code="a">Issues in clinical and cognitive neuropsychology</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">Includes bibliographical references and index</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">Turner syndrome in childhood - Marsha L. Davenport, Stephen R. Hooper and Martha Zeger -- - Klinefelter syndrome - Judith L. Ross, Gerry A. Stefanatos and David Roeltgen -- - Fragile X syndrome : the journey from genes to behavior - Kimberly M. Cornish, Andrew Levitas and Vicki Sudhalter -- - Duchenne muscular dystrophy - Veronica J. Hinton and Edward M. Goldstein -- - Neurofibromatosis - John M. Slopis and Bartlett D. Moore III -- - Cognitive and behavioral characteristics of children with chromosome 22q11.2 deletion syndrome - Tony J. Simon, Merav Burg-Malki and Doron Gothelf -- - Williams Syndrome - Carolyn B. Mervis and Colleen A. Morris -- - Congenital hypothyroidism : genetic and biochemical influences on brain development and neuropsychological functioning - Joanne F. Rovet and Rosalind Brown -- - Inborn errors of metabolism - Kevin M. Antshel and Georgianne Arnold -- - Neurodevelopmental effects of childhood exposure to heavy metals : lessons from pediatric lead poisoning - Theodore I. Lidsky, Agnes T. Heaney, Jay S. Schneider and John F. Rosen -- - Beyond the diagnosis : the process of genetic counseling - Allyn McConkie-Rosell and Julianne O'Daniel -- - From diagnosis to adaptation : optimizing family and child functioning when a genetic diagnosis is associated with mental retardation - Laraine Masters Glidden and Sarah A. Schoolcraft -- - When a genetic disorder is associated with learning disabilities - Michele M. M. Mazzocco -- - Early intervention and early childhood special education for young children with neurogenetic disorders - Deborah D. Hatton -- - The individualized education program : navigating the IEP development process - Vicki Sudhalter</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Chromosome abnormalities</subfield><subfield code="2">fast</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Developmental disabilities / Genetic aspects</subfield><subfield code="2">fast</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Neurogenetics</subfield><subfield code="2">fast</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Pediatric neuropsychology</subfield><subfield code="2">fast</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Genetic Diseases, Inborn / diagnosis</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Child</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Genetic Counseling / methods</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Heredodegenerative Disorders, Nervous System / diagnosis</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Sex Chromosome Disorders / diagnosis</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Developmental disabilities</subfield><subfield code="x">Genetic aspects</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chromosome abnormalities</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Neurogenetics</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Pediatric neuropsychology</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Neurogenetik</subfield><subfield code="0">(DE-588)4589213-1</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Entwicklungsstörung</subfield><subfield code="0">(DE-588)4014966-3</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="655" ind1=" " ind2="7"><subfield code="8">1\p</subfield><subfield code="0">(DE-588)4143413-4</subfield><subfield code="a">Aufsatzsammlung</subfield><subfield code="2">gnd-content</subfield></datafield><datafield tag="689" ind1="0" ind2="0"><subfield code="a">Entwicklungsstörung</subfield><subfield code="0">(DE-588)4014966-3</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2="1"><subfield code="a">Neurogenetik</subfield><subfield code="0">(DE-588)4589213-1</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2=" "><subfield code="8">2\p</subfield><subfield code="5">DE-604</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Mazzocco, Michèle M. M.</subfield><subfield code="e">Sonstige</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Ross, Judith L.</subfield><subfield code="e">Sonstige</subfield><subfield code="4">oth</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">http://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&db=nlabk&AN=190978</subfield><subfield code="x">Aggregator</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-4-EBA</subfield></datafield><datafield tag="999" ind1=" " ind2=" "><subfield code="a">oai:aleph.bib-bvb.de:BVB01-028546260</subfield></datafield><datafield tag="883" ind1="1" ind2=" "><subfield code="8">1\p</subfield><subfield code="a">cgwrk</subfield><subfield code="d">20201028</subfield><subfield code="q">DE-101</subfield><subfield code="u">https://d-nb.info/provenance/plan#cgwrk</subfield></datafield><datafield tag="883" ind1="1" ind2=" "><subfield code="8">2\p</subfield><subfield code="a">cgwrk</subfield><subfield code="d">20201028</subfield><subfield code="q">DE-101</subfield><subfield code="u">https://d-nb.info/provenance/plan#cgwrk</subfield></datafield><datafield tag="966" ind1="e" ind2=" "><subfield code="u">http://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&db=nlabk&AN=190978</subfield><subfield code="l">FAW01</subfield><subfield code="p">ZDB-4-EBA</subfield><subfield code="q">FAW_PDA_EBA</subfield><subfield code="x">Aggregator</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="966" ind1="e" ind2=" "><subfield code="u">http://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&db=nlabk&AN=190978</subfield><subfield code="l">FAW02</subfield><subfield code="p">ZDB-4-EBA</subfield><subfield code="q">FAW_PDA_EBA</subfield><subfield code="x">Aggregator</subfield><subfield code="3">Volltext</subfield></datafield></record></collection> |
genre | 1\p (DE-588)4143413-4 Aufsatzsammlung gnd-content |
genre_facet | Aufsatzsammlung |
id | DE-604.BV043122069 |
illustrated | Not Illustrated |
indexdate | 2024-07-10T07:18:06Z |
institution | BVB |
isbn | 0262134802 0262279320 1429477156 9780262134804 9780262279321 9781429477154 |
language | English |
oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-028546260 |
oclc_num | 144569767 |
open_access_boolean | |
owner | DE-1046 DE-1047 |
owner_facet | DE-1046 DE-1047 |
physical | 1 Online-Ressource (xiv, 507 p.) |
psigel | ZDB-4-EBA ZDB-4-EBA FAW_PDA_EBA |
publishDate | 2007 |
publishDateSearch | 2007 |
publishDateSort | 2007 |
publisher | MIT Press |
record_format | marc |
series2 | Issues in clinical and cognitive neuropsychology |
spelling | Neurogenetic developmental disorders variation of manifestation in childhood edited by Michèle M.M. Mazzocco and Judith L. Ross Cambridge, Mass. MIT Press c2007 1 Online-Ressource (xiv, 507 p.) txt rdacontent c rdamedia cr rdacarrier Issues in clinical and cognitive neuropsychology Includes bibliographical references and index Turner syndrome in childhood - Marsha L. Davenport, Stephen R. Hooper and Martha Zeger -- - Klinefelter syndrome - Judith L. Ross, Gerry A. Stefanatos and David Roeltgen -- - Fragile X syndrome : the journey from genes to behavior - Kimberly M. Cornish, Andrew Levitas and Vicki Sudhalter -- - Duchenne muscular dystrophy - Veronica J. Hinton and Edward M. Goldstein -- - Neurofibromatosis - John M. Slopis and Bartlett D. Moore III -- - Cognitive and behavioral characteristics of children with chromosome 22q11.2 deletion syndrome - Tony J. Simon, Merav Burg-Malki and Doron Gothelf -- - Williams Syndrome - Carolyn B. Mervis and Colleen A. Morris -- - Congenital hypothyroidism : genetic and biochemical influences on brain development and neuropsychological functioning - Joanne F. Rovet and Rosalind Brown -- - Inborn errors of metabolism - Kevin M. Antshel and Georgianne Arnold -- - Neurodevelopmental effects of childhood exposure to heavy metals : lessons from pediatric lead poisoning - Theodore I. Lidsky, Agnes T. Heaney, Jay S. Schneider and John F. Rosen -- - Beyond the diagnosis : the process of genetic counseling - Allyn McConkie-Rosell and Julianne O'Daniel -- - From diagnosis to adaptation : optimizing family and child functioning when a genetic diagnosis is associated with mental retardation - Laraine Masters Glidden and Sarah A. Schoolcraft -- - When a genetic disorder is associated with learning disabilities - Michele M. M. Mazzocco -- - Early intervention and early childhood special education for young children with neurogenetic disorders - Deborah D. Hatton -- - The individualized education program : navigating the IEP development process - Vicki Sudhalter Chromosome abnormalities fast Developmental disabilities / Genetic aspects fast Neurogenetics fast Pediatric neuropsychology fast Genetic Diseases, Inborn / diagnosis Child Genetic Counseling / methods Heredodegenerative Disorders, Nervous System / diagnosis Sex Chromosome Disorders / diagnosis Developmental disabilities Genetic aspects Chromosome abnormalities Neurogenetics Pediatric neuropsychology Neurogenetik (DE-588)4589213-1 gnd rswk-swf Entwicklungsstörung (DE-588)4014966-3 gnd rswk-swf 1\p (DE-588)4143413-4 Aufsatzsammlung gnd-content Entwicklungsstörung (DE-588)4014966-3 s Neurogenetik (DE-588)4589213-1 s 2\p DE-604 Mazzocco, Michèle M. M. Sonstige oth Ross, Judith L. Sonstige oth http://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&db=nlabk&AN=190978 Aggregator Volltext 1\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk 2\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk |
spellingShingle | Neurogenetic developmental disorders variation of manifestation in childhood Chromosome abnormalities fast Developmental disabilities / Genetic aspects fast Neurogenetics fast Pediatric neuropsychology fast Genetic Diseases, Inborn / diagnosis Child Genetic Counseling / methods Heredodegenerative Disorders, Nervous System / diagnosis Sex Chromosome Disorders / diagnosis Developmental disabilities Genetic aspects Chromosome abnormalities Neurogenetics Pediatric neuropsychology Neurogenetik (DE-588)4589213-1 gnd Entwicklungsstörung (DE-588)4014966-3 gnd |
subject_GND | (DE-588)4589213-1 (DE-588)4014966-3 (DE-588)4143413-4 |
title | Neurogenetic developmental disorders variation of manifestation in childhood |
title_auth | Neurogenetic developmental disorders variation of manifestation in childhood |
title_exact_search | Neurogenetic developmental disorders variation of manifestation in childhood |
title_full | Neurogenetic developmental disorders variation of manifestation in childhood edited by Michèle M.M. Mazzocco and Judith L. Ross |
title_fullStr | Neurogenetic developmental disorders variation of manifestation in childhood edited by Michèle M.M. Mazzocco and Judith L. Ross |
title_full_unstemmed | Neurogenetic developmental disorders variation of manifestation in childhood edited by Michèle M.M. Mazzocco and Judith L. Ross |
title_short | Neurogenetic developmental disorders |
title_sort | neurogenetic developmental disorders variation of manifestation in childhood |
title_sub | variation of manifestation in childhood |
topic | Chromosome abnormalities fast Developmental disabilities / Genetic aspects fast Neurogenetics fast Pediatric neuropsychology fast Genetic Diseases, Inborn / diagnosis Child Genetic Counseling / methods Heredodegenerative Disorders, Nervous System / diagnosis Sex Chromosome Disorders / diagnosis Developmental disabilities Genetic aspects Chromosome abnormalities Neurogenetics Pediatric neuropsychology Neurogenetik (DE-588)4589213-1 gnd Entwicklungsstörung (DE-588)4014966-3 gnd |
topic_facet | Chromosome abnormalities Developmental disabilities / Genetic aspects Neurogenetics Pediatric neuropsychology Genetic Diseases, Inborn / diagnosis Child Genetic Counseling / methods Heredodegenerative Disorders, Nervous System / diagnosis Sex Chromosome Disorders / diagnosis Developmental disabilities Genetic aspects Neurogenetik Entwicklungsstörung Aufsatzsammlung |
url | http://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&db=nlabk&AN=190978 |
work_keys_str_mv | AT mazzoccomichelemm neurogeneticdevelopmentaldisordersvariationofmanifestationinchildhood AT rossjudithl neurogeneticdevelopmentaldisordersvariationofmanifestationinchildhood |