Condition: Cranioectodermal dysplasia
rs199952377
in
WDR35
gene and
Cranioectodermal dysplasia
PMID 22486404
2013 Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome).
PMID 25914204
2015 Respiratory motile cilia dysfunction in a patient with cranioectodermal dysplasia.
PMID 28332779
2017 Intrafamilial phenotypic variability in a Polish family with Sensenbrenner syndrome and biallelic WDR35 mutations.