Lack of Association between Missense Variants in GRHL3 (rs2486668 and rs545809) and Susceptibility to Non-Syndromic Orofacial Clefts in a Han Chinese Population
Author:
Funder
National Natural Science Foundation of China
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference22 articles.
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2. Cleft lip and palate: understanding genetic and environmental influences;MJ Dixon;Nat Rev Genet,2011
3. Disruption of an AP-2alpha binding site in an IRF6 enhancer is associated with cleft lip;F Rahimov;Nat Genet,2008
4. Orofacial cleft risk is increased with maternal smoking and specific detoxification-gene variants;M Shi;Am J Hum Genet,2007
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2. Two rare variants reveal the significance of Grainyhead‐like 3 Arginine 391 underlying non‐syndromic cleft palate only;Oral Diseases;2022-04-19
3. Genetic markers for non-syndromic orofacial clefts in populations of European ancestry: a meta-analysis;Scientific Reports;2022-01-24
4. Association analysis of SNPs in GRHL3 , FAF1 , and KCNJ2 with NSCPO sub‐phenotypes in Han Chinese;Oral Diseases;2021-08-06
5. Association of nucleotide variants of GRHL3, IRF6, NAT2, SDC2, BCL3, and PVRL1 genes with nonsyndromic cleft lip with/without cleft palate in multigenerational families: A retrospective study;Contemporary Clinical Dentistry;2021
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