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Familial orofaciodigital syndrome type I presenting as adult polycystic kidney disease.

A three generation family with orofaciodigital syndrome type I is described. Several family members had been thought to suffer from autosomal dominant polycystic kidney disease but examination of the proband led to establishment of the correct diagnosis. The genetic implications for the offspring of...

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Bibliografski detalji
Glavni autori: Donnai, D, Kerzin-Storrar, L, Harris, R
Format: Artigo
Jezik:Inglês
Izdano: 1987
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1049894/
https://ncbi.nlm.nih.gov/pubmed/3560172
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