Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene.

Polymorphic DNA markers can now be used for presymptomatic and prenatal diagnosis of the autosomal dominant form of polycystic kidney disease (PKD). A detailed map is known for the chromosomal region around the PKD1 gene on the short arm of chromosome 16. We present here a simple, two step procedure...

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Detalhes bibliográficos
Publicado no:J Med Genet
Main Authors: Breuning, M H, Snijdewint, F G, Dauwerse, J G, Saris, J J, Bakker, E, Pearson, P L, vanOmmen, G J
Formato: Artigo
Idioma:Inglês
Publicado em: BMJ Publishing Group 1990
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1017239/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1978861/
https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.27.10.614
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