Associated Papers
MSX1 Gene Polymorphisms in Patients with non-Syndromic Cleft lip and Palate: A Tertiary Care Centre Based Case-Control Study from Central Kerala.
Jyothish A et al.
The Cleft Palate-craniofacial Journal : Official Publication of the American Cleft Palate-craniofacial Association, 2025
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
Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot project.
Cong PK et al.
Nature Communications, 2022
35618720 (PubMed )
Supplement: 41467_2022_30526_MOESM5_ESM.xlsx › Data_2
Analysis of the contribution of 129 candidate genes to thoracic aortic aneurysm or dissection of a mixed cohort of sporadic and familial cases in South China.
Li Y et al.
American Journal of Translational Research, 2021
Two novel mutations in MSX1 causing oligodontia.
Yang L et al.
Plos One, 2020
31914153 (PubMed )
Supplement: pone.0227287.s007.docx
The GenomeAsia 100K Project enables genetic discoveries across Asia.
Unknown Author
Nature, 2019
31802016 (PubMed )
Supplement: 41586_2019_1793_MOESM3_ESM.xlsx › S4b_-_Disease_Var
MSX1 mutations and associated disease phenotypes: genotype-phenotype relations.
Liang J et al.
European Journal of Human Genetics : Ejhg, 2016
Preaxial polydactyly associated with a MSX1 mutation and report of two novel mutations.
Wattanarat O et al.
American Journal of Medical Genetics. Part A, 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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