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Holder AM, Klaassens M, Tibboel D, et al. Genetic factors in congenital diaphragmatic hernia. Am J Hum Genet. 2007;80(5):825-45doi: 10.1086/513442.
Holder, A. M., Klaassens, M., Tibboel, D., de Klein, A., Lee, B., & Scott, D. A. (2007). Genetic factors in congenital diaphragmatic hernia. American journal of human genetics, 80(5), 825-45. https://doi.org/10.1086/513442
Holder, A M, et al. "Genetic factors in congenital diaphragmatic hernia." American journal of human genetics vol. 80,5 (2007): 825-45. doi: https://doi.org/10.1086/513442
Holder AM, Klaassens M, Tibboel D, de Klein A, Lee B, Scott DA. Genetic factors in congenital diaphragmatic hernia. Am J Hum Genet. 2007 May;80(5):825-45. doi: 10.1086/513442. Epub 2007 Apr 04. PMID: 17436238; PMCID: PMC1852742.
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Am J Hum Genet. 2007 May;80(5):825-45. doi: 10.1086/513442. Epub 2007 Apr 04.

Genetic factors in congenital diaphragmatic hernia.

American journal of human genetics

A M Holder, M Klaassens, D Tibboel, A de Klein, B Lee, D A Scott

Affiliations

  1. Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.

PMID: 17436238 PMCID: PMC1852742 DOI: 10.1086/513442

Abstract

Congenital diaphragmatic hernia (CDH) is a relatively common birth defect associated with high mortality and morbidity. Although the exact etiology of most cases of CDH remains unknown, there is a growing body of evidence that genetic factors play an important role in the development of CDH. In this review, we examine key findings that are likely to form the basis for future research in this field. Specific topics include a short overview of normal and abnormal diaphragm development, a discussion of syndromic forms of CDH, a detailed review of chromosomal regions recurrently altered in CDH, a description of the retinoid hypothesis of CDH, and evidence of the roles of specific genes in the development of CDH.

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