Non-Mendelian genetics in humans

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1. Verfasser: Ostrer, Harry (VerfasserIn)
Format: Buch
Sprache:English
Veröffentlicht: New York [u.a.] Oxford Univ. Press 1998
Schriftenreihe:Oxford monographs on medical genetics 35
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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
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dewey-ones 599 - Mammalia
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indexdate 2024-12-23T15:01:05Z
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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
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