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    Research 991–1000 of 1000+

    1. Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation Case reports in dermatological medicine · 2023
    2. Congenital Atrichia: A Case Report International journal of science and healthcare research · 2023
    3. Omenn syndrome in a 10-month-old male with athymia and VACTERL association Journal of allergy and clinical Immunology. Global · 2023
    4. Molecular Basis of Hereditary Hair Diseases The Keio Journal of Medicine · 2023
    5. 1426 Deletion of hoxc13 in frogs reveals key steps in the molecular evolution of cornified skin appendages 2023
    6. Dermatological diseases from a genetic perspective Medizinische Genetik · 2023
    7. Mediator 1 ablation induces enamel-to-hair lineage conversion through enhancer dynamics bioRxiv (Cold Spring Harbor Laboratory) · 2022
    8. BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations British Journal of Dermatology · 2021
    9. Clouston’s syndrome: a rare case report International Journal of Research in Dermatology · 2020
    10. The Naked (N) Mutation, Chromosome 15 2020