Genetic Studies in the Nigerian Population Implicate a MSX1 Mutation in Complex Oral Facial Clefting Disorders

BACKGROUND: Orofacial clefts are the most common malformations of the head and neck with a World-wide prevalence of 1/700 births. They are commonly divided into CL(P) and CP based on anatomical, genetic and embryological findings. A Nigerian craniofacial anomalies study “NigeriaCRAN” was set up in 2...

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Bibliografski detalji
Glavni autori: Butali, A, Mossey, P.A, Adeyemo, W.L, Jezewski, P.A, Onwuamah, C.K, Ogunlewe, M.O, Ugboko, V.I., Adejuyigbe, O, Adigun, A.I., Abdur-Rahman, L.O, Onah, I.I., Audu, R.A, Idigbe, E.O., Mansilla, M.A., Dragan, E.A, Petrin, A.L, Bullard, S.A, Uduezue, A.O., Akpata, O., Osaguona, A.O, Olasoji, H.O, Ligali, T.O, Kejeh, B.M, Iseh, K.R, Olaitan, P.B, Adebola, A.R, Efunkoya, E, Adesina, O.A, Oluwatosin, O.M, Murray, J.C
Format: Artigo
Jezik:Inglês
Izdano: 2011
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Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3206991/
https://ncbi.nlm.nih.gov/pubmed/21740177
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1597/10-133
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