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Research 61–90 of 1000+
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Hair and scalp disorders
- Hirsutism: diagnosis and treatment
- HAIR AND SYSTEMATIC DISEASE
- Congenital hair loss disorders: Rare, but not too rare
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Genetics of Alopecia
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Genetic Hair Disorders: A Review
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Causes and Management of Hypertrichosis
- Answer
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Differential expression and functionality of ATP-binding cassette transporters in the human hair follicle
- Monilethrix – Case report of a rare disease
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Alopecia Areata
- Endocrine-skin interactions
- Trichoscopy in Hair Shaft Disorders
- Molecular Genetics of Alopecias
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Secondary cicatricial and other permanent alopecias
- Evaluation of Hair Loss
- Exogen hair characterization in human scalp
- Abstracts Pt.30