Non-Mendelian genetics in humans:
Gespeichert in:
1. Verfasser: | |
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Format: | Buch |
Sprache: | English |
Veröffentlicht: |
New York [u.a.]
Oxford Univ. Press
1998
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Schriftenreihe: | Oxford monographs on medical genetics
35 |
Schlagworte: | |
Online-Zugang: | Inhaltsverzeichnis |
Beschreibung: | X, 202 S. Ill., graph. Darst. |
ISBN: | 0195068777 |
Internformat
MARC
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245 | 1 | 0 | |a Non-Mendelian genetics in humans |c Harry Ostrer |
264 | 1 | |a New York [u.a.] |b Oxford Univ. Press |c 1998 | |
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490 | 1 | |a Oxford monographs on medical genetics |v 35 | |
650 | 7 | |a Antropogenetica |2 gtt | |
650 | 4 | |a Genetic Diseases, Inborn |x genetics | |
650 | 4 | |a Genetics, Medical | |
650 | 4 | |a Human genetics | |
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650 | 4 | |a Molecular Biology | |
650 | 4 | |a Mutation | |
650 | 0 | 7 | |a Erbkrankheit |0 (DE-588)4015106-2 |2 gnd |9 rswk-swf |
650 | 0 | 7 | |a Humangenetik |0 (DE-588)4072653-8 |2 gnd |9 rswk-swf |
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Datensatz im Suchindex
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adam_text | Contents
Introduction, 3
1. Mendelian Inheritance in Humans, 5
2. The Molecular Basis of Mendelian Disease, 21
3. Deviations from the Mendelian Paradigm, 37
4. Chromosomal Transmission, 51
5. Sex Chromosome Transmission, 83
6. Mitochondrial Inheritance, 103
7. Genomic Imprinting, 125
8. Accelerated Rates of Mutation, 145
9. Viral Infection, 169
10. Human Variation: Determinism or Chance? 187
Index, 197
|
any_adam_object | 1 |
author | Ostrer, Harry |
author_facet | Ostrer, Harry |
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dewey-ones | 599 - Mammalia |
dewey-raw | 599.93/5 |
dewey-search | 599.93/5 |
dewey-sort | 3599.93 15 |
dewey-tens | 590 - Animals |
discipline | Biologie |
format | Book |
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illustrated | Illustrated |
indexdate | 2024-07-09T18:26:08Z |
institution | BVB |
isbn | 0195068777 |
language | English |
oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-008378446 |
oclc_num | 36961368 |
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owner | DE-20 DE-11 |
owner_facet | DE-20 DE-11 |
physical | X, 202 S. Ill., graph. Darst. |
publishDate | 1998 |
publishDateSearch | 1998 |
publishDateSort | 1998 |
publisher | Oxford Univ. Press |
record_format | marc |
series | Oxford monographs on medical genetics |
series2 | Oxford monographs on medical genetics |
spelling | Ostrer, Harry Verfasser aut Non-Mendelian genetics in humans Harry Ostrer New York [u.a.] Oxford Univ. Press 1998 X, 202 S. Ill., graph. Darst. txt rdacontent n rdamedia nc rdacarrier Oxford monographs on medical genetics 35 Antropogenetica gtt Genetic Diseases, Inborn genetics Genetics, Medical Human genetics Medical genetics Molecular Biology Mutation Erbkrankheit (DE-588)4015106-2 gnd rswk-swf Humangenetik (DE-588)4072653-8 gnd rswk-swf Humangenetik (DE-588)4072653-8 s Erbkrankheit (DE-588)4015106-2 s DE-604 Oxford monographs on medical genetics 35 (DE-604)BV000008339 35 HBZ Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=008378446&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
spellingShingle | Ostrer, Harry Non-Mendelian genetics in humans Oxford monographs on medical genetics Antropogenetica gtt Genetic Diseases, Inborn genetics Genetics, Medical Human genetics Medical genetics Molecular Biology Mutation Erbkrankheit (DE-588)4015106-2 gnd Humangenetik (DE-588)4072653-8 gnd |
subject_GND | (DE-588)4015106-2 (DE-588)4072653-8 |
title | Non-Mendelian genetics in humans |
title_auth | Non-Mendelian genetics in humans |
title_exact_search | Non-Mendelian genetics in humans |
title_full | Non-Mendelian genetics in humans Harry Ostrer |
title_fullStr | Non-Mendelian genetics in humans Harry Ostrer |
title_full_unstemmed | Non-Mendelian genetics in humans Harry Ostrer |
title_short | Non-Mendelian genetics in humans |
title_sort | non mendelian genetics in humans |
topic | Antropogenetica gtt Genetic Diseases, Inborn genetics Genetics, Medical Human genetics Medical genetics Molecular Biology Mutation Erbkrankheit (DE-588)4015106-2 gnd Humangenetik (DE-588)4072653-8 gnd |
topic_facet | Antropogenetica Genetic Diseases, Inborn genetics Genetics, Medical Human genetics Medical genetics Molecular Biology Mutation Erbkrankheit Humangenetik |
url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=008378446&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
volume_link | (DE-604)BV000008339 |
work_keys_str_mv | AT ostrerharry nonmendeliangeneticsinhumans |