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Research 211–240 of 1000+
- 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
- Pigmentary mosaicism: An update
- Expression of novel keratin associated protein 5 genes in the cuticle layer of human hair follicles
- Congenital atrichia with papular lesions
- Marie-unna hereditary hypotrichosis
- Monilethrix
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Familial congenital generalized hypertrichosis
- Cheveu, vieillissement et environnement : aspects cliniques épidémiologiques
- 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
- Atrichia With Papular Lesions Confirmed via Genetic Testing: A Case Report
- Human Adipose-derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Papular atrichia
- Hox demarcates regional regeneration of adult hair follicle stem cells
- Author response: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- A review of genetic researches of and rogenic alopecia
- Decision letter: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- Alopecia areata and Down syndrome: A true association and the importance of dermoscopic diagnosis
- A mouse with bad hair and poor taste
- Genetics of blond hair
- An interview Drs. Felix Brockschmidt and Markus Nöthen about the genetics of androgenetic alopecia
- Acromegaloid Facial Appearance: Case Report and Literature Review
- Primary Amenorrhoea
- ODP398 A Novel NR5A1 Gene Mutation Causing 46, XY DSD Without Adrenal Insufficiency in an Immigrant Boy from Dominican Republic