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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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| Main Authors: | , , , , , , , , , , , , , , , , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2008
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| 主題: | |
| 在線閱讀: | 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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