Congenital Diaphragmatic Hernia and Chromosome 15q26: Determination of a Candidate Region by Use of Fluorescent In Situ Hybridization and Array-Based Comparative Genomic Hybridization

Congenital diaphragmatic hernia (CDH) has an incidence of 1 in 3,000 births and a high mortality rate (33%–58%). Multifactorial inheritance, teratogenic agents, and genetic abnormalities have all been suggested as possible etiologic factors. To define candidate regions for CDH, we analyzed cytogenet...

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Main Authors:	Klaassens, M., van Dooren, M., Eussen, H. J., Douben, H., den Dekker, A. T., Lee, C., Donahoe, P. K., Galjaard, R. J., Goemaere, N., de Krijger, R. R., Wouters, C., Wauters, J., Oostra, B. A., Tibboel, D., de Klein, A.
Format:	Artigo
Sprog:	Inglês
Udgivet:	The American Society of Human Genetics 2005
Fag:	Report
Online adgang:	https://ncbi.nlm.nih.gov/pmc/articles/PMC1199376/ https://ncbi.nlm.nih.gov/pubmed/15750894
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Congenital Diaphragmatic Hernia and Chromosome 15q26: Determination of a Candidate Region by Use of Fluorescent In Situ Hybridization and Array-Based Comparative Genomic Hybridization

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