Mendelian inheritance in man: catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes
Gespeichert in:
1. Verfasser: | |
---|---|
Format: | Buch |
Sprache: | English |
Veröffentlicht: |
Baltimore u.a.
Johns Hopkins Univ. Press
1990
|
Ausgabe: | 9. ed. |
Schlagworte: | |
Beschreibung: | CLXXV, 2028 S. |
ISBN: | 0801840414 |
Internformat
MARC
LEADER | 00000nam a2200000 c 4500 | ||
---|---|---|---|
001 | BV004254162 | ||
003 | DE-604 | ||
005 | 00000000000000.0 | ||
007 | t | ||
008 | 910311s1990 |||| 00||| eng d | ||
020 | |a 0801840414 |9 0-8018-4041-4 | ||
035 | |a (OCoLC)21227425 | ||
035 | |a (DE-599)BVBBV004254162 | ||
040 | |a DE-604 |b ger |e rakddb | ||
041 | 0 | |a eng | |
049 | |a DE-19 |a DE-355 |a DE-29 | ||
050 | 0 | |a QH442.4 | |
050 | 0 | |a RB155 | |
050 | 0 | |a Z6675.M4 | |
082 | 0 | |a 016.57321 |2 20 | |
084 | |a WG 6908 |0 (DE-625)148601: |2 rvk | ||
084 | |a WG 7000 |0 (DE-625)148612: |2 rvk | ||
100 | 1 | |a McKusick, Victor A. |d 1921-2008 |e Verfasser |0 (DE-588)106492586 |4 aut | |
245 | 1 | 0 | |a Mendelian inheritance in man |b catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes |c Victor A. McKusick |
250 | |a 9. ed. | ||
264 | 1 | |a Baltimore u.a. |b Johns Hopkins Univ. Press |c 1990 | |
300 | |a CLXXV, 2028 S. | ||
336 | |b txt |2 rdacontent | ||
337 | |b n |2 rdamedia | ||
338 | |b nc |2 rdacarrier | ||
650 | 7 | |a Aangeboren afwijkingen |2 gtt | |
650 | 7 | |a Chromosomen |2 gtt | |
650 | 4 | |a Chromosomes humains - Anomalies - Catalogues | |
650 | 4 | |a Chromosomes humains - Bibliographie | |
650 | 4 | |a Chromosomes humains - Catalogues | |
650 | 4 | |a Génétique médicale - Bibliographie | |
650 | 4 | |a Génétique médicale - Dictionnaires anglais | |
650 | 7 | |a Medische genetica |2 gtt | |
650 | 4 | |a Genetic Diseases, Inborn |v Bibliography | |
650 | 4 | |a Genetic Diseases, Inborn |v Encyclopedias |x English | |
650 | 4 | |a Genetics, Medical |v Bibliography | |
650 | 4 | |a Genetics, Medical |v Encyclopedias |x English | |
650 | 4 | |a Human chromosome abnormalities |x Catalogs and collections | |
650 | 4 | |a Human chromosomes |x Catalogs and collections | |
650 | 4 | |a Medical genetics |x Bibliography | |
650 | 4 | |a Medical genetics |x Dictionaries | |
650 | 4 | |a Phenotype |v Bibliography | |
650 | 4 | |a Phenotype |v Encyclopedias |x English | |
650 | 0 | 7 | |a Mendel-Regeln |0 (DE-588)4169414-4 |2 gnd |9 rswk-swf |
650 | 0 | 7 | |a Humangenetik |0 (DE-588)4072653-8 |2 gnd |9 rswk-swf |
655 | 7 | |0 (DE-588)4006432-3 |a Bibliografie |2 gnd-content | |
655 | 7 | |0 (DE-588)4066724-8 |a Wörterbuch |2 gnd-content | |
689 | 0 | 0 | |a Humangenetik |0 (DE-588)4072653-8 |D s |
689 | 0 | 1 | |a Mendel-Regeln |0 (DE-588)4169414-4 |D s |
689 | 0 | |8 1\p |5 DE-604 | |
689 | 1 | 0 | |a Humangenetik |0 (DE-588)4072653-8 |D s |
689 | 1 | |8 2\p |5 DE-604 | |
689 | 2 | 0 | |a Humangenetik |0 (DE-588)4072653-8 |D s |
689 | 2 | |8 3\p |5 DE-604 | |
999 | |a oai:aleph.bib-bvb.de:BVB01-002646353 | ||
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 | |
883 | 1 | |8 3\p |a cgwrk |d 20201028 |q DE-101 |u https://d-nb.info/provenance/plan#cgwrk |
Datensatz im Suchindex
_version_ | 1804118450345345024 |
---|---|
any_adam_object | |
author | McKusick, Victor A. 1921-2008 |
author_GND | (DE-588)106492586 |
author_facet | McKusick, Victor A. 1921-2008 |
author_role | aut |
author_sort | McKusick, Victor A. 1921-2008 |
author_variant | v a m va vam |
building | Verbundindex |
bvnumber | BV004254162 |
callnumber-first | Q - Science |
callnumber-label | QH442 |
callnumber-raw | QH442.4 RB155 Z6675.M4 |
callnumber-search | QH442.4 RB155 Z6675.M4 |
callnumber-sort | QH 3442.4 |
callnumber-subject | QH - Natural History and Biology |
classification_rvk | WG 6908 WG 7000 |
ctrlnum | (OCoLC)21227425 (DE-599)BVBBV004254162 |
dewey-full | 016.57321 |
dewey-hundreds | 000 - Computer science, information, general works |
dewey-ones | 016 - Of works on specific subjects |
dewey-raw | 016.57321 |
dewey-search | 016.57321 |
dewey-sort | 216.57321 |
dewey-tens | 010 - Bibliography |
discipline | Allgemeines Biologie |
edition | 9. ed. |
format | Book |
fullrecord | <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>02783nam a2200721 c 4500</leader><controlfield tag="001">BV004254162</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">00000000000000.0</controlfield><controlfield tag="007">t</controlfield><controlfield tag="008">910311s1990 |||| 00||| eng d</controlfield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">0801840414</subfield><subfield code="9">0-8018-4041-4</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)21227425</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)BVBBV004254162</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-604</subfield><subfield code="b">ger</subfield><subfield code="e">rakddb</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">DE-19</subfield><subfield code="a">DE-355</subfield><subfield code="a">DE-29</subfield></datafield><datafield tag="050" ind1=" " ind2="0"><subfield code="a">QH442.4</subfield></datafield><datafield tag="050" ind1=" " ind2="0"><subfield code="a">RB155</subfield></datafield><datafield tag="050" ind1=" " ind2="0"><subfield code="a">Z6675.M4</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">016.57321</subfield><subfield code="2">20</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">WG 6908</subfield><subfield code="0">(DE-625)148601:</subfield><subfield code="2">rvk</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">WG 7000</subfield><subfield code="0">(DE-625)148612:</subfield><subfield code="2">rvk</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">McKusick, Victor A.</subfield><subfield code="d">1921-2008</subfield><subfield code="e">Verfasser</subfield><subfield code="0">(DE-588)106492586</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Mendelian inheritance in man</subfield><subfield code="b">catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes</subfield><subfield code="c">Victor A. McKusick</subfield></datafield><datafield tag="250" ind1=" " ind2=" "><subfield code="a">9. ed.</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Baltimore u.a.</subfield><subfield code="b">Johns Hopkins Univ. Press</subfield><subfield code="c">1990</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">CLXXV, 2028 S.</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">n</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="b">nc</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Aangeboren afwijkingen</subfield><subfield code="2">gtt</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Chromosomen</subfield><subfield code="2">gtt</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chromosomes humains - Anomalies - Catalogues</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chromosomes humains - Bibliographie</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chromosomes humains - Catalogues</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Génétique médicale - Bibliographie</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Génétique médicale - Dictionnaires anglais</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Medische genetica</subfield><subfield code="2">gtt</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Genetic Diseases, Inborn</subfield><subfield code="v">Bibliography</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Genetic Diseases, Inborn</subfield><subfield code="v">Encyclopedias</subfield><subfield code="x">English</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Genetics, Medical</subfield><subfield code="v">Bibliography</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Genetics, Medical</subfield><subfield code="v">Encyclopedias</subfield><subfield code="x">English</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Human chromosome abnormalities</subfield><subfield code="x">Catalogs and collections</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Human chromosomes</subfield><subfield code="x">Catalogs and collections</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Medical genetics</subfield><subfield code="x">Bibliography</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Medical genetics</subfield><subfield code="x">Dictionaries</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Phenotype</subfield><subfield code="v">Bibliography</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Phenotype</subfield><subfield code="v">Encyclopedias</subfield><subfield code="x">English</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Mendel-Regeln</subfield><subfield code="0">(DE-588)4169414-4</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Humangenetik</subfield><subfield code="0">(DE-588)4072653-8</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="655" ind1=" " ind2="7"><subfield code="0">(DE-588)4006432-3</subfield><subfield code="a">Bibliografie</subfield><subfield code="2">gnd-content</subfield></datafield><datafield tag="655" ind1=" " ind2="7"><subfield code="0">(DE-588)4066724-8</subfield><subfield code="a">Wörterbuch</subfield><subfield code="2">gnd-content</subfield></datafield><datafield tag="689" ind1="0" ind2="0"><subfield code="a">Humangenetik</subfield><subfield code="0">(DE-588)4072653-8</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2="1"><subfield code="a">Mendel-Regeln</subfield><subfield code="0">(DE-588)4169414-4</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2=" "><subfield code="8">1\p</subfield><subfield code="5">DE-604</subfield></datafield><datafield tag="689" ind1="1" ind2="0"><subfield code="a">Humangenetik</subfield><subfield code="0">(DE-588)4072653-8</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="1" ind2=" "><subfield code="8">2\p</subfield><subfield code="5">DE-604</subfield></datafield><datafield tag="689" ind1="2" ind2="0"><subfield code="a">Humangenetik</subfield><subfield code="0">(DE-588)4072653-8</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="2" ind2=" "><subfield code="8">3\p</subfield><subfield code="5">DE-604</subfield></datafield><datafield tag="999" ind1=" " ind2=" "><subfield code="a">oai:aleph.bib-bvb.de:BVB01-002646353</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="883" ind1="1" ind2=" "><subfield code="8">3\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></record></collection> |
genre | (DE-588)4006432-3 Bibliografie gnd-content (DE-588)4066724-8 Wörterbuch gnd-content |
genre_facet | Bibliografie Wörterbuch |
id | DE-604.BV004254162 |
illustrated | Not Illustrated |
indexdate | 2024-07-09T16:10:29Z |
institution | BVB |
isbn | 0801840414 |
language | English |
oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-002646353 |
oclc_num | 21227425 |
open_access_boolean | |
owner | DE-19 DE-BY-UBM DE-355 DE-BY-UBR DE-29 |
owner_facet | DE-19 DE-BY-UBM DE-355 DE-BY-UBR DE-29 |
physical | CLXXV, 2028 S. |
publishDate | 1990 |
publishDateSearch | 1990 |
publishDateSort | 1990 |
publisher | Johns Hopkins Univ. Press |
record_format | marc |
spelling | McKusick, Victor A. 1921-2008 Verfasser (DE-588)106492586 aut Mendelian inheritance in man catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes Victor A. McKusick 9. ed. Baltimore u.a. Johns Hopkins Univ. Press 1990 CLXXV, 2028 S. txt rdacontent n rdamedia nc rdacarrier Aangeboren afwijkingen gtt Chromosomen gtt Chromosomes humains - Anomalies - Catalogues Chromosomes humains - Bibliographie Chromosomes humains - Catalogues Génétique médicale - Bibliographie Génétique médicale - Dictionnaires anglais Medische genetica gtt Genetic Diseases, Inborn Bibliography Genetic Diseases, Inborn Encyclopedias English Genetics, Medical Bibliography Genetics, Medical Encyclopedias English Human chromosome abnormalities Catalogs and collections Human chromosomes Catalogs and collections Medical genetics Bibliography Medical genetics Dictionaries Phenotype Bibliography Phenotype Encyclopedias English Mendel-Regeln (DE-588)4169414-4 gnd rswk-swf Humangenetik (DE-588)4072653-8 gnd rswk-swf (DE-588)4006432-3 Bibliografie gnd-content (DE-588)4066724-8 Wörterbuch gnd-content Humangenetik (DE-588)4072653-8 s Mendel-Regeln (DE-588)4169414-4 s 1\p DE-604 2\p DE-604 3\p DE-604 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 3\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk |
spellingShingle | McKusick, Victor A. 1921-2008 Mendelian inheritance in man catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes Aangeboren afwijkingen gtt Chromosomen gtt Chromosomes humains - Anomalies - Catalogues Chromosomes humains - Bibliographie Chromosomes humains - Catalogues Génétique médicale - Bibliographie Génétique médicale - Dictionnaires anglais Medische genetica gtt Genetic Diseases, Inborn Bibliography Genetic Diseases, Inborn Encyclopedias English Genetics, Medical Bibliography Genetics, Medical Encyclopedias English Human chromosome abnormalities Catalogs and collections Human chromosomes Catalogs and collections Medical genetics Bibliography Medical genetics Dictionaries Phenotype Bibliography Phenotype Encyclopedias English Mendel-Regeln (DE-588)4169414-4 gnd Humangenetik (DE-588)4072653-8 gnd |
subject_GND | (DE-588)4169414-4 (DE-588)4072653-8 (DE-588)4006432-3 (DE-588)4066724-8 |
title | Mendelian inheritance in man catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes |
title_auth | Mendelian inheritance in man catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes |
title_exact_search | Mendelian inheritance in man catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes |
title_full | Mendelian inheritance in man catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes Victor A. McKusick |
title_fullStr | Mendelian inheritance in man catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes Victor A. McKusick |
title_full_unstemmed | Mendelian inheritance in man catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes Victor A. McKusick |
title_short | Mendelian inheritance in man |
title_sort | mendelian inheritance in man catalogs of autosomal dominant autosomal recessive and x linked phenotypes |
title_sub | catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes |
topic | Aangeboren afwijkingen gtt Chromosomen gtt Chromosomes humains - Anomalies - Catalogues Chromosomes humains - Bibliographie Chromosomes humains - Catalogues Génétique médicale - Bibliographie Génétique médicale - Dictionnaires anglais Medische genetica gtt Genetic Diseases, Inborn Bibliography Genetic Diseases, Inborn Encyclopedias English Genetics, Medical Bibliography Genetics, Medical Encyclopedias English Human chromosome abnormalities Catalogs and collections Human chromosomes Catalogs and collections Medical genetics Bibliography Medical genetics Dictionaries Phenotype Bibliography Phenotype Encyclopedias English Mendel-Regeln (DE-588)4169414-4 gnd Humangenetik (DE-588)4072653-8 gnd |
topic_facet | Aangeboren afwijkingen Chromosomen Chromosomes humains - Anomalies - Catalogues Chromosomes humains - Bibliographie Chromosomes humains - Catalogues Génétique médicale - Bibliographie Génétique médicale - Dictionnaires anglais Medische genetica Genetic Diseases, Inborn Bibliography Genetic Diseases, Inborn Encyclopedias English Genetics, Medical Bibliography Genetics, Medical Encyclopedias English Human chromosome abnormalities Catalogs and collections Human chromosomes Catalogs and collections Medical genetics Bibliography Medical genetics Dictionaries Phenotype Bibliography Phenotype Encyclopedias English Mendel-Regeln Humangenetik Bibliografie Wörterbuch |
work_keys_str_mv | AT mckusickvictora mendelianinheritanceinmancatalogsofautosomaldominantautosomalrecessiveandxlinkedphenotypes |