Associated Papers
Genotypic and phenotypic correlations in tooth agenesis: insights from WNT10A and EDA mutations in syndromic and non-syndromic forms.
Wu Y et al.
Human Genetics, 2024
Abnormal primary and permanent dentitions with ectodermal symptoms predict WNT10A deficiency.
Bergendal B et al.
Bmc Medical Genetics, 2016
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
Integrated analysis of germline and somatic variants in ovarian cancer.
Kanchi KL et al.
Nature Communications, 2014
24448499 (PubMed )
Supplement: NIHMS551112-supplement-8.xlsx › S_Data_7
Candidate gene analysis of tooth agenesis identifies novel mutations in six genes and suggests significant role for WNT and EDA signaling and allele combinations.
Arte S et al.
Plos One, 2013
23991204 (PubMed )
Supplement: pone.0073705.s002.xlsx › suppla_Table_2
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