PMID: 6540680Aug 1, 1984Paper

Pierre Robin sequence and hyperphalangy--a genetic entity (Catel-Manzke syndrome)

European Journal of Pediatrics
E Brude

Abstract

Since the first description by Catel and Manzke of hyperphalangy and clinodactyly of the index finger associated with Robin malformation sequence, seven further cases have been published. In two families more than one case occurred. Another family is presented with possibly two affected boys showing variable features of the syndrome. It is proposed that the trait is X-chromosomal, recessively inherited.

Citations

Dec 17, 2004·Clinical Dysmorphology·Rainer KoenigSigrun Fuchs
Mar 27, 1995·American Journal of Medical Genetics·A DudinA Rambaud-Cousson
Apr 15, 1993·American Journal of Medical Genetics·G N WilsonG S Brookshire
Jan 1, 1993·American Journal of Medical Genetics·D ChitayatF Halal
May 27, 2008·European Journal of Medical Genetics·Hermann ManzkeAlmuth Caliebe
Dec 7, 2014·American Journal of Human Genetics·Nadja EhmkeStefan Mundlos
Oct 1, 1986·American Journal of Medical Genetics·M RobinowJ Apesos
Mar 20, 2015·American Journal of Medical Genetics. Part a·Jesse M HunterLisa Baumbach-Reardon
Oct 18, 2003·Clinical Dysmorphology·Ratna Dua Puri, Shubha R Phadke

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