Showing 1 - 6 results of 6 for search 'Wohlfart, Sigrun', query time: 0.03s Refine Results
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  1. 1
    Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly Update

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

    Published 2023
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  2. 2
    Congenital Nail Disorders among Children with Suspected Ectodermal Dysplasias

    Congenital Nail Disorders among Children with Suspected Ectodermal Dysplasias by Maier-Wohlfart, Sigrun, Aicher, Carmen, Willershausen, Ines, Peschel, Nicolai, Meißner, Udo, Gölz, Lina, Schneider, Holm

    Published 2022
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  3. 3
    Ectodysplasin A1 Deficiency Leads to Osteopetrosis-like Changes in Bones of the Skull Associated with Diminished Osteoclastic Activity

    Ectodysplasin A1 Deficiency Leads to Osteopetrosis-like Changes in Bones of the Skull Associated with Diminished Osteoclastic Activity by Schweikl, Christine, Maier-Wohlfart, Sigrun, Schneider, Holm, Park, Jung

    Published 2022
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  4. 4
    Natural history of X-linked hypohidrotic ectodermal dysplasia: a 5-year follow-up study

    Natural history of X-linked hypohidrotic ectodermal dysplasia: a 5-year follow-up study by Wohlfart, Sigrun, Meiller, Ralph, Hammersen, Johanna, Park, Jung, Menzel-Severing, Johannes, Melichar, Volker O., Huttner, Kenneth, Johnson, Ramsey, Porte, Florence, Schneider, Holm

    Published 2020
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  5. 5
    Mutationsspektrum und Genotyp-Phänotyp-Korrelationen bei hypohidrotischer ektodermaler Dysplasie = Mutational spectrum and genotype-phenotype correlations in subjects with hypohidrotic ectodermal dysplasia

    Mutationsspektrum und Genotyp-Phänotyp-Korrelationen bei hypohidrotischer ektodermaler Dysplasie = Mutational spectrum and genotype-phenotype correlations in subjects with hypohidr... by Wohlfart, Sigrun

    Published 2017
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  6. 6
    No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia

    No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia by Körber, Laura, Schneider, Holm, Fleischer, Nicole, Maier-Wohlfart, Sigrun

    Published 2021
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