Search
forResearch 10 of 928
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- PA15 Becker naevus syndrome associated with a mosaic pathogenic variant in <i>ACTB</i>
- Pigmentary mosaicism: An update
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Hypopigmented Mycosis Fungoides Treated with 308 nm Excimer Laser
- Fibromodulin reduces scar formation in adult cutaneous wounds by eliciting a fetal-like phenotype
- Effects of gamma rays on the regeneration of murine hair follicles in the natural hair cycle
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Menkes Syndrome Presenting as Myoclonic Seizures: Neuroimaging and EEG Observations
- Hyperpigmented Upper Eyelid: A Clue to the Diagnosis of Facial Lichen Planus Pigmentosus in a Patient with Frontal Fibrosing Alopecia
Learn
— no results
Try a deeper search in learn →Community
— no results
Try a deeper search in community →