Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies.
作者信息
Ribeiro-Bicudo Lucilene Arilho, Quiezi Rodrigo G, Guion-Almeida Maria Leine, Legnaro Chiara, Richieri-Costa Antonio
机构信息
Department of Clinical Genetics, Hospital of Rehabilitation of Craniofacial Anomalies, University of São Paulo, Bauru, SP, Brazil.
出版信息
Am J Med Genet A. 2012 May;158A(5):1233-5. doi: 10.1002/ajmg.a.35305. Epub 2012 Apr 11.
PMID:22496059
Abstract
摘要
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Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies.排除患有额鼻发育不全、胼胝体发育不全、基底脑膨出和眼部异常综合征患者的TGIF、ALX3和ALX4基因突变。
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