Novel IRF6 mutations in families with Van Der Woude syndrome and popliteal pterygium syndrome from sub-Saharan Africa

Orofacial clefts (OFC) are complex genetic traits that are often classified as syndromic or nonsyndromic clefts. Currently, there are over 500 types of syndromic clefts in the Online Mendelian Inheritance in Man (OMIM) database, of which Van der Woude syndrome (VWS) is one of the most common (accoun...

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Hlavní autoři: Butali, Azeez, Mossey, Peter A, Adeyemo, Wasiu L, Eshete, Mekonen A, Gaines, LauRen A, Even, Dee, Braimah, Ramat O, Aregbesola, Babatunde S, Rigdon, Jennifer V, Emeka, Christian I, James, Olutayo, Ogunlewe, Mobolanle O, Ladeinde, Akinola L, Abate, Fikre, Hailu, Taye, Mohammed, Ibrahim, Gravem, Paul E, Deribew, Milliard, Gesses, Mulualem, Adeyemo, Adebowale A, Murray, Jeffrey C
Médium: Artigo
Jazyk:Inglês
Vydáno: BlackWell Publishing Ltd 2014
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Original Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4049366/
https://ncbi.nlm.nih.gov/pubmed/24936515
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.66
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