Selection for carriers of recessive diseases: A common phenomenon?
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference19 articles.
1. Mutations in CYP1B1, the Gene for Cytochrome P4501B1, Are the Predominant Cause of Primary Congenital Glaucoma in Saudi Arabia
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1. Neuroprotective effects respond to cerebral ischemia without susceptibility to HB-tumorigenesis in VHL heterozygous knockout mice;Molecular Carcinogenesis;2017-06-30
2. Genetic diseases in the Tunisian population;American Journal of Medical Genetics Part A;2010-12-28
3. The mystery of the mystery of common genetic diseases;Biology & Philosophy;2009-10-15
4. Multiple mutations responsible for frequent genetic diseases in isolated populations;European Journal of Human Genetics;2007-01-10
5. ARH mutations and hypercholesterolaemia in Sardinia;The Lancet;2002-09
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