TBX22 mutations are a frequent cause of cleft palate

A. C. B MARCANO; K DOUDNEY; P STONIER; C BRAYBROOK; R SQUIRES; M. A PATTON; M. M LEES; A RICHIERI-COSTA; A. C LIDRAL; J. C MURRAY; G. E MOORE

doi:10.1136/jmg.2003.010868

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TBX22 mutations are a frequent cause of cleft palate

Letter/Communication

Open access

TBX22 mutations are a frequent cause of cleft palate

A. C. B MARCANO, K DOUDNEY, P STONIER, C BRAYBROOK, R SQUIRES, M. A PATTON, M. M LEES, A RICHIERI-COSTA, A. C LIDRAL, J. C MURRAY, …

Journal of medical genetics, Vol.41(1), pp.68-74

2004

DOI: 10.1136/jmg.2003.010868

PMCID: PMC1757272

PMID: 14729838

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Abstract

Biological and medical sciences

Medical sciences

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

Otorhinolaryngology. Stomatology

Non tumoral diseases

Details

Title: Subtitle: TBX22 mutations are a frequent cause of cleft palate
Creators: A. C. B MARCANO - Institute of Reproductive and Developmental Biology, Imperial College London, Du Cane Road, London W12 ONN, United Kingdom
K DOUDNEY - Institute of Reproductive and Developmental Biology, Imperial College London, Du Cane Road, London W12 ONN, United Kingdom
P STONIER - Institute of Reproductive and Developmental Biology, Imperial College London, Du Cane Road, London W12 ONN, United Kingdom
C BRAYBROOK - Institute of Reproductive and Developmental Biology, Imperial College London, Du Cane Road, London W12 ONN, United Kingdom
R SQUIRES - Medical Genetics Unit, St George's Hospital Medical School, Tooting, London SW17 0RE, United Kingdom
M. A PATTON - Medical Genetics Unit, St George's Hospital Medical School, Tooting, London SW17 0RE, United Kingdom
M. M LEES - Medical Genetics Unit, St George's Hospital Medical School, Tooting, London SW17 0RE, United Kingdom
A RICHIERI-COSTA - Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, Bauru, Sao Paulo, Brazil
A. C LIDRAL - Department of Orthodontics, University of Iowa, IA, United States
J. C MURRAY - Department of Pediatrics, University of Iowa, IA, United States
G. E MOORE - Institute of Reproductive and Developmental Biology, Imperial College London, Du Cane Road, London W12 ONN, United Kingdom
Resource Type: Letter/Communication
Publication Details: Journal of medical genetics, Vol.41(1), pp.68-74
DOI: 10.1136/jmg.2003.010868
PMID: 14729838
PMCID: PMC1757272
NLM abbreviation: J Med Genet
ISSN: 0022-2593
eISSN: 1468-6244
Publisher: BMJ; London
Language: English
Date published: 2004
Academic Unit: Anatomy and Cell Biology; Stead Family Department of Pediatrics; Epidemiology; Pediatric Dentistry; Craniofacial Anomalies Research Center; Dental Research
Record Identifier: 9984025440002771

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