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Research 391–420 of 1000+
- A missense mutation in Lama3 causes androgen alopecia
- Pearly Pinna Papules in a Young Female
- Cutaneous Tumours of Pilar Origin with Associated Syndromes
- A RARE CASE OF CHRONIC ACRODERMATITIS ENTEROPATHICA PERSISTING AND RECURRING IN THE ADULT AGE
- SELF-CARE OF MALE PATTERN HAIR LOSS – Selfcare Journal
- Polycystic ovary syndrome
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Molecular mechanisms of asymmetric divisions in mammary stem cells
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Recently Identified Forms of Epidermolysis Bullosa
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Epidemiological study of prostate cancer (EPICAP): a population-based case–control study in France
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Symptomatic zinc deficiency in a full-term breast-fed infant
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Autoimmune gastritis and parietal cell reactivity in two children with abnormal intestinal permeability
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Diseases of Periocular Hair
- Early-onset androgenetic alopecia in China: a descriptive study of a large outpatient cohort
- Disorders of hair
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- The involvement of androgens in human hair growth
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study
- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog