Linkage analysis for the diagnosis of autosomal dominant polycystic kidney disease, and for the determination of genetic heterogeneity in Italian families
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1991.tb03098.x/fullpdf
Reference36 articles.
1. Linkage study of a large family with autosomal dominant polycystic kidney disease with reduced expression. Absence of linkage to the PKD1 locus;Bachner;Hum. Genet.,1990
2. A locus on chromosome 11p with multiple restriction site polymorphisms;Barker;Am. J. Hum. Genet.,1984
3. Age at clinical onset and at ultrasonographic detection of adult polycystic kidney disease: data for genetic counselling;Bear;Am. J. Med. Genet.,1984
4. Improved early diagnosis of adult polycystic kidney disease with flanking DNA markers;Breuning;Lancet,1987
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1. Genetic analysis of 20 families with autosomal dominant adult polycystic kidney disease from South West Thames Region;Clinical Genetics;2008-04-23
2. A family with autosomal dominant polycystic kidney disease not linked to chromosome 16p13.3;Clinical Genetics;2008-04-23
3. Genetic Dissection of Complex Traits;Focus;2006-08
4. Lexikon der Syndrome und Fehlbildungen;Lexikon der Syndrome und Fehlbildungen;1999
5. Rapid DNA-based prenatal diagnosis by genetic linkage in three families with Alport's syndrome;American Journal of Kidney Diseases;1997-08
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