De Novo interstitial deletion 13q33.3q34 in a male patient with double outlet right ventricle, microcephaly, dysmorphic craniofacial findings, and motor and developmental delay-Reference-Cited by-同舟云学术

De Novo interstitial deletion 13q33.3q34 in a male patient with double outlet right ventricle, microcephaly, dysmorphic craniofacial findings, and motor and developmental delay

Published:2015-03-21 Issue:5 Volume:167 Page:1134-1141
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

McMahon Colin J¹,Breathnach Colm¹,Betts David R²,Sharkey Freddie H³,Greally Marie T²

Affiliation:

1. Department of Pediatric Cardiology; Our Lady's Children's Hospital; Crumlin Dublin Ireland

2. National Centre for Medical Genetics; Our Lady's Children's Hospital, Crumlin; Dublin Ireland

3. Ion Torrent; Thermo Fisher Scientific; Paisley United Kingdom

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference35 articles.

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4. Role of corin in trophoblast invasion and uterine spiral artery remodeling in pregnancy;Cui;Nature,2012

5. The phenotypic spectrum of ZIC3 mutations includes isolated d-transposition of the great arteries and double outlet right ventricle;D'Alessandro;Am J Med Genet A,2013

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