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Research 991–1000 of 1000+
- Roles of MED1 in Quiescence of Hair Follicle Stem Cells and Maintenance of Normal Hair Cycling
- Monilethrix: A rare hereditary condition
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Many Paths to Alopecia via Compromised Regeneration of Hair Follicle Stem Cells
- Exploring the efficacy of testosterone undecanoate in male children with 5α‐reductase deficiency
- Epstein-Barr virus associated with high-grade B-cell lymphoma in nude severe combined immunodeficiency
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Acne Syndromes and Mosaicism
- Bilateral nevus comedonicus of the eyelids: An unusual cause of ptosis and ectropion
- Zebrafish Model of Hereditary Pigmentary Disorders