Associated Papers
Genetic analysis of transcription factors in dopaminergic neuronal development in Parkinson's disease.
Zhao Y et al.
Chinese Medical Journal, 2024
37341647 (PubMed )
Supplement: cm9-137-450-s001.pdf
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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