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Research 481–510 of 1000+
- [An infant with short stature and red cheeks (Rothmund-Thomson syndrome)].
- Fully functional salivary gland regeneration as a next-generation regenerative therapy
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- Papillon-Lefévre Syndrome: A Rare Case Report and a Brief Review of Literature
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Co-option of Hair Follicle Keratins into Amelogenesis Is Associated with the Evolution of Prismatic Enamel: A Hypothesis
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- Alopecia triangularis congenita in combination with androgenetic alopecia
- Your good health : how to stay well, and what to do when you're not
- Kartagener Syndrome With Ectodermal Anomalies in An Adolescent Female: A Case Report
- Phytochemical Investigation of Tamarix aphylla (L.) Karst: A Plant of Medicinal Value from Gujarat, India
- Structural and Pigmentary Characteristics of the Skin in Hairless Dog Breeds
- Stable isotope analyses of carbon and nitrogen in hair keratin of suspected man-eating wolves from 1880s
- Short anagen hair syndrome is caused by mutations in the <i>WNT10A</i> gene and has a genetic overlap with male pattern hair loss
- Feed Management and Nutritional Status of Gibbons (Symphalangus Syndactylus Raffles, 1821) at Tegal Alur Animal Rescue Center, Jakarta
- PA05 A rare case of cardiocutaneous syndrome in a young child
- Case Report: 7 Year-Old Saudi Female with Monilethrix
- Sparse Hair on the Scalp
- Clouston’s syndrome: a rare case report
- ORAL CHRONIC ULCER: A DIAGNOSIS CHALLENGE
- Stem Cell Treatment in Hair Diseases
- Moniletherix
- Hypotrichosis congenita of Marie Unna
- Malassezia spp. Overgrowth in a Chinchilla Cat
- Mult-trait analysis of GWAS - Perceived youtfulness - UKBB
- Mult-trait analysis of GWAS - Perceived youtfulness - UKBB
- The Black identity, hair product use, and breast cancer scale
- The blastema and epimorphic regeneration in mammals
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Nuclear Factor I-C Regulates TGF-β-dependent Hair Follicle Cycling*