Condition: SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder)


rs372993798 in WNT10A gene and SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder) PMID 19559398 2009 WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.

PMID 21143469 2011 Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum.

rs121908119 in WNT10A;LOC107984111 gene and SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder) PMID 25629078 2015 Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds.

PMID 24702986 2014 Dento-maxillo-facial phenotype and implants-based oral rehabilitation in Ectodermal Dysplasia with WNT10A gene mutation: report of a case and literature review.

PMID 19559398 2009 WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.

PMID 24398796 2014 Variability in dentofacial phenotypes in four families with WNT10A mutations.

PMID 24902757 2014 Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome.

PMID 23167694 2013 Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis.