Genetic factors in esophageal atresia, tracheo-esophageal fistula and the VACTERL association: Roles for FOXF1 and the 16q24.1 FOX transcription factor gene cluster, and review of the literature-Reference-Cited by-同舟云学术

Genetic factors in esophageal atresia, tracheo-esophageal fistula and the VACTERL association: Roles for FOXF1 and the 16q24.1 FOX transcription factor gene cluster, and review of the literature

Published:2010-01 Issue:1 Volume:53 Page:6-13
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Shaw-Smith Charles

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference60 articles.

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3. Analysis of the phenotypic abnormalities in lymphoedema–distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24;Brice;J. Med. Genet.,2002

4. Autosomal dominant stapes ankylosis with broad thumbs and toes, hyperopia, and skeletal anomalies is caused by heterozygous nonsense and frameshift mutations in NOG, the gene encoding noggin;Brown;Am. J. Hum. Genet.,2002

5. Genetic players in esophageal atresia and tracheoesophageal fistula;Brunner;Curr. Opin. Genet. Dev.,2005

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