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Research 511–540 of 1000+
- 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
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- 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
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- 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
- A review of genetic researches of and rogenic alopecia
- Alopecia areata and Down syndrome: A true association and the importance of dermoscopic diagnosis
- A mouse with bad hair and poor taste
- ANDROGENIC ALOPECIA: PATHOGENETIC MECHANISMS AND THERAPEUTIC APPROACHES
- Genetics of blond hair
- Fine Mapping and Identifying the Mutation Gene of snthr -1Bao ScantHair Mouse
- Screening of Sheep Fibroblast Cell Line with the Spider Dragline Silk Protein Gene
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS
- Letter To Editor-Alopecia universalis in Down syndrome: Response totherapy