Novel evidence of association with NSCL/P was shown for SNPs in FOXF2 gene in an Asian population

BACKGROUND: The forkhead box F2 gene (FOXF2) located in chromosome 6p25.3 has been shown to play a crucial role in palatal development in mouse and rat models. To date, no evidence of linkage or association has been reported for this gene in humans with oral clefts. METHODS: Allelic transmission dis...

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Vydáno v:Birth Defects Res A Clin Mol Teratol
Hlavní autoři: Bu, Lingxue, Chen, Qianqian, Wang, Hong, Zhang, Tianxiao, Hetmanski, Jacqueline B., Schwender, Holger, Parker, Margaret, Chou, Yah-Huei Wu, Yeow, Vincent, Chong, Samuel S., Zhang, Bo, Jabs, Ethylin Wang, Scott, Alan F., Beaty, Terri H.
Médium: Artigo
Jazyk:Inglês
Vydáno: 2015
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Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5180447/
https://ncbi.nlm.nih.gov/pubmed/26278207
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/bdra.23413
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