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Research 61–90 of 1000+
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Monilethrix in pattern distribution in siblings: Diagnosis by trichoscopy
- Dermatoscopy of hair shaft disorders
- Keratins: the hair shaft's backbone revealed
- Keratin gene mutations in disorders of human skin and its appendages
- Trichoscopy in genetic hair shaft abnormalities
- Genetic Hair Disorders: A Review
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- AN UPDATE OF HAIR SHAFT DISORDERS
- Hair shaft disorders in children – An update
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Molecular Genetics of Alopecias
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Hair loss in children.
- Hair and Nail Relationship
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- The Significance of Scalp Involvement in Pemphigus: A Literature Review
- Beyond Expectations
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Short anagen syndrome
- Hair Loss in Children
- Unruly hair
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
- Diseases of Periocular Hair
- Hair loss and its management in children
- Advances in Hair Diseases
- Trichodystrophies: A hair-raising differential diagnosis