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Research 30 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
- Lentiginosis within plaques of linear atrophoderma of Moulin: a twin-spotting phenomenon?
- The effects of gamma rays on the regeneration of hair follicles are carried over to later hair cycles
- Obstetric and Gynecologic Dermatology
- LITERATURE REVIEW
- Skin Semiology and Grading Scales
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Spectrum of Phenotypes Associated with Human MC1R Variations
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Integrative skin phenotypic and transcriptomic analyses reveal candidate genes for coat color and fiber length in four Chinese goat breeds (<i>Capra hircus</i>)
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- Topical niacinamide 4% and desonide 0.05% for treatment of axillary hyperpigmentation: a randomized, double-blind, placebo-controlled study
- Changes in Characteristics of Murine Hair Follicles and Tissue Stem Cells Throughout Life
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- New clinico‐genetic classification of trichothiodystrophy