Please use this identifier to cite or link to this item:
Title: Schilbach-Rott syndrome in a third family: Further delineation of an autosomal dominant trait
Author: Becerra-Solano, L.E.
Casillas-Avila, M.P.
Diaz-Rodriguez, M.
Nastasi-Catanese, J.A.
Toscano-Flores, J.J.
Ramirez-Duenas, M.D.L.
Issue Date: 2007
Abstract: We describe a father-son Mexican pair with typical features of Schilbach-Rott syndrome (SRS): ocular hypotelorism, cleft palate, hypospadias (only in the child), and microcephaly. This observation documents for the first time a male to male transmission and therefore confirms that the SRS is inherited as an autosomal dominant trait with variable expressivity.
Appears in Collections:Producción científica UdeG (prueba)

Files in This Item:
There are no files associated with this item.

Items in RIUdeG are protected by copyright, with all rights reserved, unless otherwise indicated.