Associated Papers
The oligodontia phenotype in a X-linked hypohidrotic ectodermal dysplasia patient with a novel EVC2 variant.
Wu Y et al.
Heliyon, 2024
Dual Diagnosis of Ellis-van Creveld Syndrome and Hearing Loss in a Consanguineous Family.
Vona B et al.
Molecular Syndromology, 2017
Ellis-van Creveld Syndrome: Mutations Uncovered in Lebanese Families.
Valencia M et al.
Case Reports in Genetics, 2015
[Occlusal reconstruction of a patient with hypohidrotic ectodermal dysplasia].
Zeng Y et al.
Hua Xi Kou Qiang Yi Xue Za Zhi = Huaxi Kouqiang Yixue Zazhi = West China Journal of Stomatology, 2013
Two novel heterozygous mutations of EVC2 cause a mild phenotype of Ellis-van Creveld syndrome in a Chinese family.
Shen W et al.
American Journal of Medical Genetics. Part A, 2011
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