Sigrun Wohlfart
3PUBLICATIONS
0CO-AUTHORS
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Publications (3)
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|Feb 24, 2021
No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia.Laura Körber, Holm Schneider, Nicole Fleischer
|Jan 12, 2020
Natural history of X-linked hypohidrotic ectodermal dysplasia: a 5-year follow-up study.Sigrun Wohlfart, Ralph Meiller, Johanna Hammersen
|Jan 10, 2019
Variants of the ectodysplasin A1 receptor gene underlying homozygous cases of autosomal recessive hypohidrotic ectodermal dysplasia.Sigrun Wohlfart, Holm Schneider
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