Congenital Diaphragmatic Hernia Interval on Chromosome 8p23.1 Characterized by Genetics and Protein Interaction Networks
Chromosome 8p23.1 is a common hotspot associated with major congenital malformations, including congenital diaphragmatic hernia (CDH) and cardiac defects. We present findings from high-resolution arrays in patients who carry a loss (n =18) or a gain (n =1) of sub-band 8p23.1. We confirm a region inv...
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Asıl Yazarlar: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Materyal Türü: | Metin |
Dil: | İngilizce |
Baskı/Yayın Bilgisi: |
2012
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Konular: | |
Online Erişim: | https://pmc.ncbi.nlm.nih.gov/articles/PMC3761361/ https://pubmed.ncbi.nlm.nih.gov/23165946 http://dx.doi.org/10.1002/ajmg.a.35665 |
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