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ROR2 gene is associated with risk of non-syndromic cleft palate in an Asian population

BACKGROUND: The receptor tyrosine kinase-like orphan receptor 2 (ROR2) gene has been recently shown to play important roles in palatal development in animal models and resides in the chromosomal region linked to non syndromic cleft lip with or without cleft palate in humans. The aim of this study wa...

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Detalhes bibliográficos
Main Authors: WANG, Hong, Hetmanski, Jacqueline B., Ruczinski, Ingo, Liang, Kung Yee, Fallin, M. Daniele, Redett, Richard J., Raymond, Gerald V., Wu Chou, Yah-Huei, Chen, Philip Kuo-Ting, Yeow, Vincent, Chong, Samuel S., Cheah, Felicia SH, Jabs, Ethylin Wang, Scott, Alan F., Beaty, Terri H.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3384720/
https://ncbi.nlm.nih.gov/pubmed/22490406
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