Associated Papers
Orodental malformations associated with human MSX1 sequence variants.
Wang YL et al.
Journal of the American Dental Association (1939), 2024
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
Biallelic variants/mutations of IL1RAP in patients with steroid-sensitive nephrotic syndrome.
Niitsuma S et al.
International Immunology, 2020
MSX1 mutations and associated disease phenotypes: genotype-phenotype relations.
Liang J et al.
European Journal of Human Genetics : Ejhg, 2016
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