Autosomal dominant syndrome of mental retardation, hypotelorism, and cleft palate resembling Schilbach–Rott syndrome

Author:

Shkalim Vered,Baris Hagit N.,Gal Gavriel,Gleiss Ruth,Calderon Shlomo,Wessels Marja,Maat-Kievit Anneke,Menten Björn,De Baere Elfride,Hennekam Raoul C.M.,Schirmacher Anja,Bale Sherri,Shohat Mordechai,Willems Patrick J.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference19 articles.

1. Hereditary recurrent brachial plexus neuropathy with dysmorphic features;Airaksinen;Acta Neurol Scand,1985

2. Asymmetrical skull, ptosis, hypertelorism, high nasal bridge, clefting, umbilical anomalies, and skeletal anomalies in sibs: Is Carnevale syndrome a separate entity?;Al Kaissi;Am J Med Genet Part A,2007

3. Schilbach-Rott syndrome in a third family: Further delineation of an autosomal dominant trait;Becerra-Solano;Genet Couns,2007

4. Schilbach-Rott/blepharofacioskeletal syndrome in a Brazilian patient;De Carvalho;Am J Med Genet Part A,2008

5. The fronto-ocular syndrome: Second mother-daughter case;Descartes;Clin Genet,2004

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