Integrated Genomic Analyses in Bronchopulmonary Dysplasia

OBJECTIVE: To identify single nucleotide polymorphisms (SNPs) and pathways associated with bronchopulmonary dysplasia (BPD) because O(2) requirement at 36 weeks’ post-menstrual age risk is strongly influenced by heritable factors. STUDY DESIGN: A genome-wide scan was conducted on 1.2 million genotyp...

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Vydáno v:J Pediatr
Hlavní autoři: Ambalavanan, Namasivayam, Cotten, C. Michael, Page, Grier P., Carlo, Waldemar A., Murray, Jeffrey C., Bhattacharya, Soumyaroop, Mariani, Thomas J., Cuna, Alain C., Faye-Petersen, Ona M., Kelly, David, Higgins, Rosemary D.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2014
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4344889/
https://ncbi.nlm.nih.gov/pubmed/25449221
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jpeds.2014.09.052
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