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CNV analysis in 169 patients with bladder exstrophy-epispadias complex
BACKGROUND: The bladder exstrophy-epispadias complex (BEEC) represents the severe end of the congenital uro-rectal malformation spectrum. Initial studies have implicated rare copy number variations (CNVs), including recurrent duplications of chromosomal region 22q11.21, in BEEC etiology. METHODS: To...
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| Pubblicato in: | BMC Med Genet |
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| Autori principali: | , , , , , , , , , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2016
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4852408/ https://ncbi.nlm.nih.gov/pubmed/27138190 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-016-0299-x |
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