Three GLI2 mutations combined potentially underlie non‐syndromic cleft lip with or without cleft palate in a Chinese pedigree

BACKGROUND: Nonsyndromic cleft lip with or without cleft palate (NSCL/P) is the most common craniofacial birth defect. Its etiology is complex and it has a lifelong influence on affected individuals. Despite many studies, the pathogenic gene alleles are not completely clear. Here, we recruited a Chi...

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Dettagli Bibliografici
Pubblicato in:Mol Genet Genomic Med
Autori principali: Meng, Peiqi, Zhao, Huaxiang, Huang, Wenbin, Zhang, Yunfan, Zhong, Wenjie, Zhang, Mengqi, Jia, Peizeng, Zhou, Zhibo, Maimaitili, Gulibaha, Chen, Feng, Zhang, Jieni, Lin, Jiuxiang
Natura: Artigo
Lingua:Inglês
Pubblicazione: John Wiley and Sons Inc. 2019
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Original Articles
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6732289/
https://ncbi.nlm.nih.gov/pubmed/31386309
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.714
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