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Research 61–90 of 1000+
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- Symmetrical acrokeratoderma: A peculiar entity in China? Clinicopathologic and immunopathologic study of 34 new cases
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
- Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- The X Factor in Immunity: Sex Differences Shaped by the X Chromosome
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Immunolocalization of telomerases in human hairs identifies proliferating cells in the bulb matrix and outer root sheath
- Bloom's syndrome–‐a first report from India
- Pigmentary mosaicism: An update
- Case Report: Disorder of Sexual Development in a Chinese Crested Dog With XX/XY Leukocyte Chimerism and Mixed Cell Testicular Tumors
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- British Hair and Nail Society
- Androgen receptors and their biology
- Cutaneous signals of immune system disease
- Krtap11-1, a hair keratin-associated protein, as a possible crucial element for the physical properties of hair shafts
- Dermatologic care of patients with differences of sex development
- Keratosis Follicularis Squamosa in Unilateral Buttock: A Case Report and Review of Literature in China
- The biology and genetics of curly hair
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- High Frequency of Symptomatic Zinc Deficiency in Infants in Northern Ethiopia
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Clinical Case Notes. Malignant melanoma in eviscerated eyeball
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- Rheumatoid arthritis and gouty arthritis in an adult patient with Down's syndrome
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- The Skin and Subcutaneous Tissues