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Research 991–1000 of 1000+
- Curtailing PCOS
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia.
- PSEUDOPELADE: AN INHERITED ALOPECIA
- Hair Shaft Dysplasias
- Conditional Knockout in Mice Reveals the Critical Roles of Ppp2ca in Epidermis Development
- Loose Anagen Syndrome: A Retrospective Chart Review of 37 Cases
- Androgens and hair: a biological paradox
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome