Nonsynonymous variants in MYH9 and ABCA4 are the most frequent risk loci associated with nonsyndromic orofacial cleft in Taiwanese population

Author:

Peng Hsiu-Huei,Chang Nai-Chung,Chen Kuo-Ting,Lu Jang-Jih,Chang Pi-Yueh,Chang Shih-Cheng,Wu-Chou Yah-Huei,Chou Yi-Ting,Phang Wanni,Cheng Po-Jen

Funder

Chang Gung Memorial Hospital , Linkou Medical Center, Taoyuan, Taiwan

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Reference35 articles.

1. Yuan Q, Blanton SH, Hecht JT. Genetic causes of nonsyndromic cleft lip with or without cleft palate. Adv Otorhinolaryngol. 2011;70:107–13.

2. Mossey PA, Modell B. Epidemiology of oral clefts 2012: an international perspective. Front Oral Biol. 2012;16:1–18.

3. Croen LA, Shaw GM, Wasserman CR, et al. Racial and ethnic variations in the prevalence of orofacial clefts in California, 1983–1992. Am J Med Genet. 1998;79:42–7.

4. Christensen K, Juel K, Herskind AM, et al. Long term follow up study of survival associated with cleft lip and palate at birth. BMJ. 2004;328:1405.

5. Dai L, Zhu J, Mao M, et al. Time trends in oral clefts in Chinese newborns: data from the Chinese National Birth Defects Monitoring Network. Birth Defects Res A Clin Mol Teratol. 2010;88:41–7.

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