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    Research 10 of 319

    1. BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations British Journal of Dermatology · 2021
    2. A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome Indian dermatology online journal · 2023
    3. In the Empire of Images: Preface to the Tenth Anniversary Edition University of California Press eBooks · 2003 · 3 citations
    4. The Potential Teeth Bleaching and Halitosis Prevention Effects of Pediococcus inopinatus THK-30, a Kimchi-Derived Lactic Acid Bacterium: In Vitro Study Journal of functional biomaterials · 2024
    5. Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia American Journal of Human Genetics · 2007 · 109 citations
    6. A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene Clinical Case Reports · 2025
    7. EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia Genes · 2024
    8. Evo Devo of the Vertebrates Integument Journal of developmental biology · 2023 · 4 citations
    9. Molecular basis of hypohidrotic ectodermal dysplasia: an update Journal of Applied Genetics · 2015 · 85 citations
    10. Orai1 expression pattern in tooth and craniofacial ectodermal tissues and potential functions during ameloblast differentiation Developmental Dynamics · 2015 · 15 citations
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