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    Research 10 of 77

    1. Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i> The Journal of Dermatology · 2017 · 5 citations
    2. WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes American journal of human genetics · 2009 · 197 citations
    3. The fundamentals of WNT10A Differentiation · 2025 · 6 citations
    4. Inherited Disorders of the Hair Elsevier eBooks · 2013 · 2 citations
    5. Trichoscopy in Hair Shaft Disorders Dermatologic Clinics · 2018 · 36 citations
    6. <i>WNT10A</i> , dermatology and dentistry British Journal of Dermatology · 2021 · 30 citations
    7. Hypotrichosis in a child with olmsted syndrome Indian Dermatology Online Journal · 2018
    8. Molecular pathology of skin adnexal tumours Histopathology · 2021 · 16 citations
    9. Diseases of Periocular Hair Survey of Ophthalmology · 2011 · 7 citations
    10. Pili Torti: A Feature of Numerous Congenital and Acquired Conditions Journal of clinical medicine · 2021 · 9 citations
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