Familial risk of oral clefts by morphological type and severity: population based cohort study of first degree relatives
Author:
Publisher
BMJ
Subject
General Engineering
Cited by 164 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. The potential up-regulation risk of 3′ UTR SNP (rs10787760 G > A) for the VAX1 gene is associated with NSCLP in the northwest Chinese population;Gene;2024-09
2. Role of MTHFR, IRF6, PAX7 and TP63 SNPs in susceptibility to non‐syndromic orofacial cleft, a candidate gene study in a Portuguese population;Orthodontics & Craniofacial Research;2024-07-25
3. Single-Nucleotide Polymorphisms in WNT Genes in Patients with Non-Syndromic Orofacial Clefts in a Polish Population;Diagnostics;2024-07-17
4. Risk factors and the severity of defect in patients with cleft lip and palate;International Journal of Pediatric Otorhinolaryngology;2024-06
5. Genome-wide study of gene-by-sex interactions identifies risks for cleft palate;2024-05-03
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