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    1. Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family Acta Scientific Paediatrics · 2023
    2. Hypertrichosis in Childhood Turkish Journal of Dermatology · 2018 · 1 citations
    3. More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players Journal of Investigative Dermatology · 2006 · 35 citations
    4. Two Cases of Hypertrichosis Cubiti Actas Dermo-Sifiliográficas · 2007 · 2 citations
    5. A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family British Journal of Dermatology · 2000 · 36 citations
    6. Faun tail nevus: A series of 15 cases and their management with Intense Pulse Light 2018 · 3 citations
    7. An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis Journal of Investigative Dermatology · 2006 · 97 citations
    8. Current Genetics in Hair Diseases InTech eBooks · 2013 · 1 citations
    9. Marie-unna hereditary hypotrichosis International Journal of Trichology · 2014 · 4 citations
    10. Hipertricose generalizada exuberante em um lactente: relato de caso Residência Pediátrica · 2024
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