Localization of a Gene for Nonsyndromic Renal Hypodysplasia to Chromosome 1p32-33

Nonsyndromic defects in the urinary tract are the most common cause of end-stage renal failure in children and account for a significant proportion of adult nephropathy. The genetic basis of these disorders is not fully understood. We studied seven multiplex kindreds ascertained via an index case wi...

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Detalhes bibliográficos
Main Authors: Sanna-Cherchi, Simone, Caridi, Gianluca, Weng, Patricia L., Dagnino, Monica, Seri, Marco, Konka, Anita, Somenzi, Danio, Carrea, Alba, Izzi, Claudia, Casu, Domenica, Allegri, Landino, Schmidt-Ott, Kai M., Barasch, Jonathan, Scolari, Francesco, Ravazzolo, Roberto, Ghiggeri, Gian Marco, Gharavi, Ali G.
Formato: Artigo
Idioma:Inglês
Publicado em: The American Society of Human Genetics 2007
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1821099/
https://ncbi.nlm.nih.gov/pubmed/17273976
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