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Research 61–90 of 1000+
- Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss
- Genetic correlation analysis does not associate male pattern baldness with COVID-19
- Genetic and hormonal influence on SARS-CoV-2-infection susceptibility
- Fine Mapping and Identifying the Mutation Gene of snthr -1Bao ScantHair Mouse
- A review of genetic researches of and rogenic alopecia
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- The Sex-Linked Histocompatibility Antigens
- SEXUAL DIMORPHISM IN MAMMALS
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Bloom's syndrome–‐a first report from India
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Polycystic ovary syndrome (PCOS) trilogy: a translational and clinical review
- Treatment of alopecia areata: “What is new on the horizon?”
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Molecular basis of androgen insensitivity
- Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis
- The role of mutations on gene AR, in androgenetic alopecia syndrome
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Sex- or Gender-specific Differences in the Clinical Presentation, Outcome, and Treatment of SARS-CoV-2
- Comment on: The Gabrin sign
- Androgen receptors and their biology
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- This Month in the Journal
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Characterization and Chromosomal Localization of Human Hair-Specific Keratin Genes and Comparative Expression During the Hair Growth Cycle
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless