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    Research 61–90 of 1000+

    1. Novel<i>PAX</i><i>9</i>mutation associated with syndromic tooth agenesis European Journal of Oral Sciences · 2013 · 20 citations
    2. Hair Shaft Fracture in a Young Athlete: A Rare Case Report of Acquired Trichorrhexis Nodosa Cureus · 2024
    3. Contents Pediatric Clinics of North America · 2014
    4. Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice Journal of Biological Chemistry · 2002 · 15 citations
    5. RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome The American Journal of Human Genetics · 2012 · 112 citations
    6. Ectodermal Dysplasia: Variable Expressions Indian Journal of Dermatology · 2025
    7. A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2 Revista Paulista de Pediatria · 2023
    8. Frizzled Receptors in Development and Disease 2016 · 114 citations
    9. FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program Frontiers in Immunology · 2013 · 69 citations
    10. Poster Presentations Australasian Journal of Dermatology · 2021 · 25 citations
    11. Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins IntechOpen eBooks · 2021 · 1 citations
    12. Keratin 17 null mice exhibit age- and strain-dependent alopecia Genes & Development · 2002 · 122 citations
    13. Hair loss and its management in children Expert Review of Dermatology · 2011 · 5 citations
    14. Adams–Oliver syndrome: new evidence in variable expressivity? International Journal of Dermatology · 2013
    15. Nutrition and Hair Dermatologic Clinics · 2012 · 98 citations
    16. To grow or not to grow: Hair morphogenesis and human genetic hair disorders Seminars in Cell & Developmental Biology · 2013 · 43 citations
    17. Congenital hypotrichosis due to short anagen British Journal of Dermatology · 2000 · 42 citations
    18. <i>WNT10A</i> , dermatology and dentistry British Journal of Dermatology · 2021 · 30 citations
    19. Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs PLoS ONE · 2012 · 28 citations
    20. Pregnancy and Skin The Journal of Obstetrics and Gynecology of India · 2012 · 26 citations
    21. The usefulness of dermoscopy in canine pattern alopecia: a descriptive study Veterinary Dermatology · 2016 · 16 citations
    22. Congenital atrichia and hypotrichosis World Journal of Pediatrics · 2011 · 11 citations
    23. 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
    24. Hair shaft structures in EDAR induced ectodermal dysplasia BMC Medical Genetics · 2015 · 5 citations
    25. A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia Archives of Dermatological Research · 2015 · 2 citations
    26. Inherited Disorders of the Hair Elsevier eBooks · 2013 · 2 citations
    27. Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment 2018 · 1 citations
    28. Dermoscopy — 4th Conference of the Section of Dermoscopy and Other Skin Imaging Techniques (DiTOS) of the Polish Dermatological Society — Abstracts Forum Dermatologicum · 2026
    29. Telogen Effluvium, Diagnosis and Management: A Narrative Review International Journal of Biomedicine · 2023
    30. Visual Diagnosis: The Case of the Balding Preschooler Pediatrics in Review · 2017