PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI

Conference proceeding

Peer reviewed

Lucilene ARILHO RIBEIRO, Jeffrey C MURRAY and Antonio RICHIERI-COSTA

American journal of medical genetics. Part A, Vol.140(23), pp.2584-2586

Facial and oral structures: molecular perspectives, October 22-23, 2005

2006

DOI: 10.1002/ajmg.a.31369

PMID: 17001668

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Neurology

Malformations of the nervous system

Otorhinolaryngology. Stomatology

Non tumoral diseases

Medical genetics

Biological and medical sciences

Medical sciences

Facial bones, jaws, teeth, parodontium: diseases, semeiology

Title: Subtitle: PTCH mutations in four brazilian patients with holoprosencephaly and in one with holoprosencephaly-like features and normal MRI
Creators: Lucilene ARILHO RIBEIRO - Serviço de Genética, Hospital de Reabilitacao de Anomalias Craniofaciais, Universidade de São Paulo, Bauru, São Paulo, Brazil
Jeffrey C MURRAY - Department of Pediatrics, University of Iowa, Iowa City, IA, United States
Antonio RICHIERI-COSTA - Serviço de Genética, Hospital de Reabilitacao de Anomalias Craniofaciais, Universidade de São Paulo, Bauru, São Paulo, Brazil
Resource Type: Conference proceeding
Publication Details: American journal of medical genetics. Part A, Vol.140(23), pp.2584-2586
Conference: Facial and oral structures: molecular perspectives, October 22-23, 2005
DOI: 10.1002/ajmg.a.31369
PMID: 17001668
NLM abbreviation: Am J Med Genet A
ISSN: 1552-4825
eISSN: 1552-4833
Publisher: Wiley-Liss; Hoboken, NJ
Language: English
Date published: 2006
Academic Unit: Anatomy and Cell Biology; Stead Family Department of Pediatrics; Epidemiology; Pediatric Dentistry; Craniofacial Anomalies Research Center; Dental Research
Record Identifier: 9984025373202771

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