Childhood onset autosomal dominant polycystic kidney disease in sibs: clinical picture and recurrence risk. German Working Group on Paediatric Nephrology (Arbeitsgemeinschaft fur Padiatrische Nephrologie.

Author:

Zerres K,Rudnik-Schoneborn S,Deget F

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference25 articles.

1. Bilateral polycystic disease of the kidneys. A follow-up of two hundred eighty-four patients and their families;Dalgaard, O.Z.;Acta Med Scand,1957

2. Autosomal dominant polycystic renal disease;Kaplan, B.S.; Rabin, I.; Nogrady, M.B.; Drummond, K.N.,1977

3. Prenatal diagnosis of an early manifestation of autosomal dominant adult-type polycystic kidney disease;Zerres, K.; Weiss, H.; Bulla, M.; Roth, B.;Lancet,1982

4. Autosomal dominant polycystic kidney disease in childhood: a longitudinal study;Sedman, A.; Bell, P.; Manco-Johnson, M.;Kidney Int,1987

5. Polycystic kidney disease in children: differential diagnosis between the dominantly and recessively inherited forms;Kaariainen, H.,1988

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