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Non-mendelian genetics in humans

Author: Harry Ostrer
Publisher: New York : Oxford University Press, 1998.
Series: Oxford monographs on medical genetics, no. 35.
Edition/Format:   Print book : EnglishView all editions and formats
Summary:

Rediscovered at the turn of the century, Mendel's laws were found to be applicable to humans but were fraught with problems. This text shows how some of these problems can be explained by incomplete  Read more...

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Material Type: Internet resource
Document Type: Book, Internet Resource
All Authors / Contributors: Harry Ostrer
ISBN: 0195068777 9780195068771
OCLC Number: 36961368
Description: x, 202 pages : illustrations ; 24 cm.
Contents: 1. Mendelian Inheritance in Humans --
2. The Molecular Basis of Mendelian Disease --
3. Deviations from the Mendelian Paradigm --
4. Chromosomal Transmission --
5. Sex Chromosome Transmission --
6. Mitochondrial Inheritance --
7. Genomic Imprinting --
8. Accelerated Rates of Mutation --
9. Viral Infection --
10. Human Variation: Determinism or Chance?
Series Title: Oxford monographs on medical genetics, no. 35.
Responsibility: Harry Ostrer.
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<http:\/\/experiment.worldcat.org\/entity\/work\/data\/596716#Topic\/antropogenetica<\/a>> # Antropogenetica<\/span>\n\u00A0\u00A0\u00A0\u00A0a \nschema:Intangible<\/a> ;\u00A0\u00A0\u00A0\nschema:name<\/a> \"Antropogenetica<\/span>\"@en<\/a> ;\u00A0\u00A0\u00A0\u00A0.\n\n\n<\/div>\n
<http:\/\/experiment.worldcat.org\/entity\/work\/data\/596716#Topic\/erbkrankheit<\/a>> # Erbkrankheit<\/span>\n\u00A0\u00A0\u00A0\u00A0a \nschema:Intangible<\/a> ;\u00A0\u00A0\u00A0\nschema:name<\/a> \"Erbkrankheit<\/span>\"@en<\/a> ;\u00A0\u00A0\u00A0\u00A0.\n\n\n<\/div>\n
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