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Sequence variants in the HLX gene at chromosome 1q41-1q42 in patients with diaphragmatic hernia
Congenital diaphragmatic hernia (CDH) is a common birth defect for which few causative genes have been identified. Several candidate regions containing genes necessary for normal diaphragm development have been identified, including a 4–5 Mb deleted region at chromosome 1q41–1q42 from which the caus...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2874832/ https://ncbi.nlm.nih.gov/pubmed/19459883 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1399-0004.2009.01182.x |
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