Associated Papers
Exome Sequencing Reveals the Genetic Architecture of Non-syndromic Orofacial Clefts and Identifies BOC as a Novel Causal Gene.
He Q et al.
Advanced Science (weinheim, Baden-wurttemberg, Germany), 2025
40464334 (PubMed )
Supplement: ADVS-12-e12073-s004.xlsx › Sheet1
Regional patterns of genetic variants in expanded carrier screening: a next-generation sequencing pilot study in Fujian Province, China.
Guo D et al.
Frontiers in Genetics, 2025
40421383 (PubMed )
Supplement: Table1.xlsx › Table_S3
PAX9 mutations and genetic synergism in familial tooth agenesis.
Chu KY et al.
Annals of the New York Academy of Sciences, 2023
Early diagnosis of Schöpf-Schulz-Passarge syndrome by whole-exome sequencing: the first Chinese case.
Ren JN et al.
Journal of the European Academy of Dermatology and Venereology : Jeadv, 2022
The Changing Landscape in the Genetic Etiology of Human Tooth Agenesis.
Williams MA et al.
Genes, 2018
Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds.
Yang J et al.
Molecular Genetics & Genomic Medicine, 2015
25629078 (PubMed )
Supplement: mgg30003-0040-sd1.docx
Tricho-odonto-onycho-dermal dysplasia and WNT10A mutations.
Kantaputra P et al.
American Journal of Medical Genetics. Part A, 2014
WNT10A mutations also associated with agenesis of the maxillary permanent canines, a separate entity.
Kantaputra P et al.
American Journal of Medical Genetics. Part A, 2014
Select a paper to view details