Cantú Syndrome Is Caused by Mutations in ABCC9-Reference-Cited by-同舟云学术

Cantú Syndrome Is Caused by Mutations in ABCC9

Published:2012-06 Issue:6 Volume:90 Page:1094-1101
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

van Bon Bregje W.M.,Gilissen Christian,Grange Dorothy K.,Hennekam Raoul C.M.,Kayserili Hülya,Engels Hartmut,Reutter Heiko,Ostergaard John R.,Morava Eva,Tsiakas Konstantinos,Isidor Bertrand,Le Merrer Martine,Eser Metin,Wieskamp Nienke,de Vries Petra,Steehouwer Marloes,Veltman Joris A.,Robertson Stephen P.,Brunner Han G.,de Vries Bert B.A.,Hoischen Alexander

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference33 articles.

1. Cantu syndrome in a woman and her two daughters: Further confirmation of autosomal dominant inheritance and review of the cardiac manifestations;Grange;Am. J. Med. Genet. A.,2006

2. Autosomal dominant inheritance in Cantú syndrome (congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly);Lazalde;Am. J. Med. Genet.,2000

3. Cantú syndrome: report of nine new cases and expansion of the clinical phenotype;Scurr;Am. J. Med. Genet. A.,2011

4. Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: Cantú syndrome;Robertson;Am. J. Med. Genet.,1999

5. A distinct osteochondrodysplasia with hypertrichosis- Individualization of a probable autosomal recessive entity;Cantú;Hum. Genet.,1982

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