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Research 991–1000 of 1000+
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Zinc: an undervalued microelement in research and treatment
- Clouston’s Syndrome-A Case Report
- Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings
- Clouston’s syndrome: a rare case report
- Autoimmune polyendocrine syndrome type 1 a case report from Bangladesh
- The relevance of collagen XVII expression in epidermal differentiation and proliferation
- Nail lichen planus in a patient with alopecia totalis
- Going Beyond Hair: Seven Simple Actions We Can Take to Help Prevent Major Illness in Our Hair Transplant Patients