Parental α 1-antitrypsin (PI) types and meiotic nondisjunction in the aetiology of Down syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1981.tb01037.x/fullpdf
Reference21 articles.
1. Alpha-1-antitrypsin (Pi)-types in recurrent miscarriages;Aarskog;Clin. Genet.,1978
2. Protease inhibitor (Pi) phenotypes in chromosome aberrations;Aarskog;J. med. Genet.,1970
3. Alpha-1-anti-trypsin (Pi) types in Down's syndrome;Arnaud;Clin. Genet.,1976
4. Functional capacity of genetic variants of α1-anti-trypsin;Billingsley;Amer. J. hum. Genet.,1980
5. Increased frequency of heterozygotes for α1-antitrypsin variants in individuals with either sex chromosome mosaicism or trisomy 21;Fineman;Nature,1976
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1. Ethical and social aspects of risk predictions;Clinical Genetics;2008-04-23
2. Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndrome;Human Genetics;1989-01
3. Prenatal Diagnosis of Chromosome Abnormalities;Genetic Disorders and the Fetus;1986
4. Parental origin of autosomal trisomies;Annals of Human Genetics;1984-05
5. Origin of nondisjunction in trisomy 21 syndrome: All studies compiled, parental age analysis, and international comparisons;American Journal of Medical Genetics;1983-09
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