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    Research 181–210 of 601

    1. Focal Dermal Hypoplasia Associated With Lymphedema: A Case Report From Saudi Arabia Curēus · 2023
    2. Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia Children · 2023 · 4 citations
    3. 190 A cross-sectional study evaluating skin, hair, nail and bone disease in patients with focal dermal hypoplasia Journal of Investigative Dermatology · 2016 · 1 citations
    4. Left Testicular Hypoplasia and Right Cryptorchid Testes Seminoma in a German Shepherd Dog The Indian Journal of Animal Reproduction · 2025
    5. 1465 Optimization/characterization of a Focal Dermal Hypoplasia mouse model to test potential treatments 2018
    6. A case report of a novel homozygote mutation causing severe Leydig cell hypoplasia: insights in the coexistence of nonsense mutation and polymorphism in the same LHCGR gene locus Experimental and Clinical Endocrinology & Diabetes · 2012
    7. Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome Journal of Clinical Investigation · 2022 · 9 citations
    8. Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum Neurodegenerative Diseases · 2018 · 7 citations
    9. Hypotrichosis and nail dysplasia: A novel hidrotic ectodermal dysplasia Australasian Journal of Dermatology · 2004 · 21 citations
    10. Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets JDR Clinical & Translational Research · 2017 · 12 citations
    11. Dental manifestations in Vitamin D dependent rickets Type II with Alopecia: a short pictorial case report SVU-International Journal of Medical Sciences · 2025
    12. Role of <i>foxn1</i> in <i>Xenopus laevis</i> thymopoiesis. 2022
    13. Toxicological Responses in Keratinocyte Interfollicular Stem Cells 2018
    14. Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance Open Archive (Karolinska Institutet) · 2011
    15. An Outbreak of Alopecia in Newborn Piglets Journal of the Japan Veterinary Medical Association · 1980
    16. Altered skin development and impaired proliferative and inflammatory responses in transgenic mice overexpressing the glucocorticoid receptor The FASEB Journal · 2001 · 92 citations
    17. DKK1 Mediated Inhibition of Wnt Signaling in Postnatal Mice Leads to Loss of TEC Progenitors and Thymic Degeneration PLOS ONE · 2010 · 56 citations
    18. Over-expression of thymosin beta4 promotes abnormal tooth development and stimulation of hair growth The International Journal of Developmental Biology · 2009 · 34 citations
    19. Sox21 Regulates Anapc10 Expression and Determines the Fate of Ectodermal Organ iScience · 2020 · 22 citations
    20. Becker’s Nevus Syndrome in a Pediatric Female Patient Case reports in pediatrics · 2016 · 7 citations
    21. P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss PloS one · 2022 · 5 citations
    22. Becker's Nevus Syndrome Journal of pediatric neurology · 2018 · 4 citations
    23. Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion Journal of Human Immunity · 2025 · 1 citations
    24. Skin abnormality and hairloss: the reproductive endocrinological viewpoint Medical Journal of Indonesia · 2004
    25. X linked mental retardation. Journal of Medical Genetics · 1991 · 79 citations
    26. Widespread porokeratotic adnexal ostial nevus: Clinical features and proposal of a new name unifying porokeratotic eccrine ostial and dermal duct nevus and porokeratotic eccrine and hair follicle nevus Journal of the American Academy of Dermatology · 2009 · 60 citations
    27. Effectiveness of Anastrozole and Cyproterone Acetate in Two Brothers with Familial Male Precocious Puberty Journal of Pediatric Endocrinology and Metabolism · 2008 · 21 citations
    28. Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl 2011 · 6 citations
    29. 068 Association of systemic involvement with skin morphology assessed by multiphoton microscopy in pseudoxanthoma elasticum Journal of Investigative Dermatology · 2021
    30. Congenital and Hereditary Skin Diseases 2018