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Research 121–150 of 1000+
- Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- The hair shaft: normality, abnormality, and genetics
- Atrichia with papular lesions
- Disease causing homozygous variants in the human hairless gene
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family
- Congenital atrichia with papular lesions
- Marie-unna hereditary hypotrichosis
- Monilethrix
- <i>FOXN1</i> Duplication and Congenital Hypertrichosis
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- The first broad replication study of SNPs and a pilot genome‐wide association study for androgenetic alopecia in Asian populations
- Frontal Fibrosing Alopecia
- Banded Scalp Hair with an Unusual Glistening Appearance in a Teenager: A Quiz
- Familial congenital generalized hypertrichosis
- Cheveu, vieillissement et environnement : aspects cliniques épidémiologiques
- Alopecia Areata is associated with MICA and an extended HLA haplotype
- Natural variation in trichome density and biochemistry in Antirrhinum
- Monilethrix: Beaded hair and hypotrichosis in a child
- Immunolocalization of telomerases in human hairs identifies proliferating cells in the bulb matrix and outer root sheath
- Congenital Atrichia: A Case Report
- Atrichia With Papular Lesions Confirmed via Genetic Testing: A Case Report
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Papular atrichia
- Hox demarcates regional regeneration of adult hair follicle stem cells