Associated Papers
Nonsynonymous variants in MYH9 and ABCA4 are the most frequent risk loci associated with nonsyndromic orofacial cleft in Taiwanese population.
Peng HH et al.
Bmc Medical Genetics, 2016
Identification of Novel Variants in the PVRL1 Gene in Patients With Nonsyndromic Cleft Lip With or Without Cleft Palate.
Oner DA et al.
Genetic Testing and Molecular Biomarkers, 2016
Mutation analysis of PVRL1 in patients with non-syndromic cleft of the lip and/or palate in Guangdong.
Shu SY et al.
Genetics and Molecular Research : Gmr, 2015
Evaluating rare coding variants as contributing causes to non-syndromic cleft lip and palate.
Leslie EJ et al.
Clinical Genetics, 2013
PVRL1 as a candidate gene for nonsyndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in southern Han Chinese patients.
Cheng HQ et al.
Dna and Cell Biology, 2012
Study of the poliovirus receptor related-1 gene in Thai patients with non-syndromic cleft lip with or without cleft palate.
Tongkobpetch S et al.
International Journal of Oral and Maxillofacial Surgery, 2008
PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations.
Avila JR et al.
American Journal of Medical Genetics. Part A, 2006
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