Variant: rs199952377 

    present in Gene: WDR35
    present in Chromosome: 2
    Position on Chromosome: 19941796
    Alleles of this Variant: A/C

rs199952377 in WDR35 gene and CRANIOECTODERMAL DYSPLASIA 2 PMID 25914204 2015 Respiratory motile cilia dysfunction in a patient with cranioectodermal dysplasia.

PMID 22486404 2013 Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome).

PMID 28332779 2017 Intrafamilial phenotypic variability in a Polish family with Sensenbrenner syndrome and biallelic WDR35 mutations.

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.

rs199952377 in WDR35 gene and SHORT-RIB THORACIC DYSPLASIA 7 WITH OR WITHOUT POLYDACTYLY PMID 28332779 2017 Intrafamilial phenotypic variability in a Polish family with Sensenbrenner syndrome and biallelic WDR35 mutations.

PMID 25914204 2015 Respiratory motile cilia dysfunction in a patient with cranioectodermal dysplasia.

PMID 22486404 2013 Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome).