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The prevalence, penetrance, and expressivity of etiologic IRF6 variants in orofacial clefts patients from sub‐Saharan Africa

BACKGROUND: Orofacial clefts are congenital malformations of the orofacial region, with a global incidence of one per 700 live births. Interferon Regulatory Factor 6 (IRF6) (OMIM:607199) gene has been associated with the etiology of both syndromic and nonsyndromic orofacial clefts. The aim of this s...

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Vydáno v:Mol Genet Genomic Med
Hlavní autoři: Gowans, Lord Jephthah Joojo, Busch, Tamara D., Mossey, Peter A., Eshete, Mekonen A., Adeyemo, Wasiu L., Aregbesola, Babatunde, Donkor, Peter, Arthur, Fareed K. N., Agbenorku, Pius, Olutayo, James, Twumasi, Peter, Braimah, Rahman, Oti, Alexander A., Plange‐Rhule, Gyikua, Obiri‐Yeboah, Solomon, Abate, Fikre, Hoyte‐Williams, Paa E., Hailu, Taye, Murray, Jeffrey C., Butali, Azeez
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2017
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5370218/
https://ncbi.nlm.nih.gov/pubmed/28361103
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.273
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