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    Research 10 of 1000+

    1. 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
    2. Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome The American Journal of Human Genetics · 2012 · 71 citations
    3. PA33 When bones speak through nails: insights from a paediatric case series British Journal of Dermatology · 2025
    4. Hair and Nail Relationship Skinmed · 2005 · 21 citations
    5. Comparative Anatomy of Mouse and Human Nail Units The Anatomical Record · 2013 · 55 citations
    6. Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review Indian Journal of Dermatology · 2016 · 13 citations
    7. Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay American Journal of Medical Genetics Part A · 2003 · 5 citations
    8. The skin manifestations in end-stage renal disease patients in Jordan, single-center experience BMC Nephrology · 2025
    9. PA05 A rare case of cardiocutaneous syndrome in a young child 2023
    10. A 9-month-old infant with severe scalp dermatosis Journal of the American Academy of Dermatology · 2016
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    Community 1 of 6

    1. The final nail in the coffin. PP405 is confirmed JXL069. Reddit · 26 Jul 2026
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