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Research 511–540 of 1000+
- BRITISH ASSOCIATION OF DERMATOLOGY.
- Damage of hair follicle stem cells and alteration of keratin expression in external radiation-induced acute alopecia
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Finding bald spots on chromosome 20p11
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- 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
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Polycystic ovary syndrome (PCOS) trilogy: a translational and clinical review
- Treatment of alopecia areata: “What is new on the horizon?”
- Bloom's syndrome–‐a first report from India
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- 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
- This Month in the Journal