Suchergebnisse - Wohlfart, Sigrun

Mutationsspektrum und Genotyp-Phänotyp-Korrelationen bei hypohidrotischer ektodermaler Dysplasie: = Mutational spectrum and genotype-phenotype correlations in subjects with hypohidrotic ectodermal dysplasia

von Wohlfart, Sigrun

Ectodysplasin A1 Deficiency Leads to Osteopetrosis-like Changes in Bones of the Skull Associated with Diminished Osteoclastic Activity

von Schweikl, Christine, Maier-Wohlfart, Sigrun, Schneider, Holm, Park, Jung

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Natural history of X-linked hypohidrotic ectodermal dysplasia: a 5-year follow-up study

von Wohlfart, Sigrun, Meiller, Ralph, Hammersen, Johanna, Park, Jung, Menzel-Severing, Johannes, Melichar, Volker O., Huttner, Kenneth, Johnson, Ramsey, Porte, Florence, Schneider, Holm

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Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly Update

von Peschel, Nicolai, Wright, John T., Koster, Maranke I., Clarke, Angus J., Tadini, Gianluca, Fete, Mary, Hadj-Rabia, Smail, Sybert, Virginia P., Norderyd, Johanna, Maier-Wohlfart, Sigrun, Fete, Timothy J., Pagnan, Nina, Visinoni, Atila F., Schneider, Holm

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Congenital Nail Disorders among Children with Suspected Ectodermal Dysplasias

von Maier-Wohlfart, Sigrun, Aicher, Carmen, Willershausen, Ines, Peschel, Nicolai, Meißner, Udo, Gölz, Lina, Schneider, Holm

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No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia

von Körber, Laura, Schneider, Holm, Fleischer, Nicole, Maier-Wohlfart, Sigrun

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