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Research 61–90 of 1000+
- Index of Suspicion
- A Clinical Genetics-Driven Dual Diagnosis of Prader–Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Genome-Wide Associations with Body and Fleece Weight in United States Sheep
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?
- Androgens and hair loss
- Improving human forensics through advances in genetics, genomics and molecular biology
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- SUN-069 A 14 Year Old Female with Primary Amenorrhea
- Sex- or Gender-specific Differences in the Clinical Presentation, Outcome, and Treatment of SARS-CoV-2
- Characterization of Bsk mice: I. The Bsk mutation does not involve a recombination of cornea-specific keratin 12 and skin-specific hair keratin genes.
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene
- Klinefelter syndrome and chronic leg ulcers
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- THE PATTERN OF SILVER-RUSSELL SYNDROME: OWN OBSERVATION
- Histopathological Analysis on keratin2-6 g Expression in Hair Mutant Mouse Hague
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- The Majority of Multipotent Epidermal Stem Cells Do Not Protect Their Genome by Asymmetrical Chromosome Segregation
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Transcriptomic analysis of human skin wound healing and rejuvenation following ablative fractional laser treatment
- Proteomic analysis of balding and non-balding mesenchyme-derived dermal papilla cells from androgenetic alopecia patients using on-line two-dimensional reversed phase-reversed phase LC–MS/MS
- Integrated single-cell chromatin and transcriptomic analyses of peripheral immune cells in patients with alopecia areata
- Comparative analysis of stemness between dermal papilla cells and human dermalstem/progenitor cells
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Intraovarian vascular enhancement via stromal injection of platelet-derived growth factors: Exploring subsequent oocyte chromosomal status and in vitro fertilization outcomes
- Analysis of genetic polymorphisms of steroid 5α-reductase type 1 and 2 genes in Korean men with androgenetic alopecia