Associated Papers
Genetic investigations on singleton school aged children reveal novel variants and new candidate genes for hearing loss.
Khan H et al.
Scientific Reports, 2024
39271758 (PubMed )
Supplement: 41598_2024_71407_MOESM1_ESM.xlsx › HLMS06_het
Two novel mutations in MSX1 causing oligodontia.
Yang L et al.
Plos One, 2020
31914153 (PubMed )
Supplement: pone.0227287.s007.docx
MSX1 mutations and associated disease phenotypes: genotype-phenotype relations.
Liang J et al.
European Journal of Human Genetics : Ejhg, 2016
Evaluating rare coding variants as contributing causes to non-syndromic cleft lip and palate.
Leslie EJ et al.
Clinical Genetics, 2013
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