Bilateral renal agenesis in 2 male sibs born to consanguineous parents.

Author:

Schinzel A,Homberger C,Sigrist T

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference9 articles.

1. Nuclear sex and genital malformation in 48 cases of renal agenesis, with especial reference to nonspecific female pseudohermaphroditism;Carpenter, R.J.; Potter, E.L.;American Journal ofObstetrics and Gynecology,1959

2. Potter syndrome. Nonrenal features induced by oligoamnios;Fantel, A.G.; Shepard, T.H.;American Journal of Diseases ofChildren,1975

3. Potter-Syndrom (Nierenagenesie) mit chromosomaler Aberration beim Patienten und Mosaik beim Vater;Ferrandez, A.; Schmid, W.;Helvetica Paediatrica Acta,1971

4. Unilateral and bilateral renal agenesis in monoamniotic twins;Mauer, S.M.; Dobrin, R.S.; Vernier, R.L.;Journal of Pediatrics,1974

5. A 4psyndrome. A case report;Mikelsaar, A.V.N.; Lazjuk, G.J.; Lurie, I.W.; Tiiiir, S.; Kaosaar, M.E.; Mikelsaar, R.; Loolaid, V.E.;Humangenetik,1973

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1. Congenital Anomalies of the Kidney and Urinary Tract;Emery and Rimoin's Principles and Practice of Medical Genetics;2013

2. Renal anomalies in family members of infants with bilateral renal agenesis/adysplasia;Pediatric Nephrology;2007-01

3. Genetic bases of renal agenesis in the ACI rat: mapping of Renag1 to chromosome 14;Mammalian Genome;2006-07

4. The ‘skipped generation’ phenomenon in a family with renal agenesis;Ultrasound in Obstetrics and Gynecology;2004-08-16

5. Recurrent Potter`s syndrome in a consanguineous marriage;Journal of Obstetrics and Gynaecology;1998-01

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