Differential Parental Transmission of Markers in RUNX2 Among Cleft Case-Parent Trios From Four Populations

Isolated cleft lip with or without cleft palate (CL/P) is among the most common human birth defects, with a prevalence around 1 in 700 live births. The Runt-related transcription factor 2 (RUNX2) gene has been suggested as a candidate gene for CL/P based largely on mouse models; however, no human st...

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Autors principals: Sull, Jae Woong, Liang, Kung-Yee, Hetmanski, Jacqueline B., Fallin, Margaret Daniele, Ingersoll, Roxann G., Park, Jiwan, Wu-Chou, Yah-Huei, Chen, Philip K., Chong, Samuel S., Cheah, Felicia, Yeow, Vincent, Park, Beyoung Yun, Jee, Sun Ha, Jabs, Ethylin Wang, Redett, Richard, Jung, Euiju, Ruczinski, Ingo, Scott, Alan F., Beaty, Terri H.
Format: Artigo
Idioma:Inglês
Publicat: 2008
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2841966/
https://ncbi.nlm.nih.gov/pubmed/18357615
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/gepi.20323
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