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Research 301–330 of 1000+
- A Comprehensive Review of GWASs of Human Hair Traits
- Genomic Analysis of Trichotillomania
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- The first broad replication study of SNPs and a pilot genome‐wide association study for androgenetic alopecia in Asian populations
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Glucocorticoid Resistance Syndrome in 2 Patients With Diverse Genotype
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- Hair follicle group and skin follicle population of Australian Merino sheep
- Association between the D19S884 marker at the insulin receptor gene locus and polycystic ovary syndrome
- Fine mapping of the human <i>AR/EDA2R</i> locus in androgenetic alopecia
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- ALOPECIA AREATA-A CLINICAL ANALYSIS
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- Characterisation of Four New Genes in the Ovine KAP19 Family
- Perspectives of Kennedy's disease
- Identification of the Ovine Keratin-Associated Protein 22-1 (KAP22-1) Gene and Its Effect on Wool Traits
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Frontal Fibrosing Alopecia – a review and a practical guide for clinicians
- Molecular cloning, characterization, and expression of sheep FGF5 gene
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Nonalcoholic fatty liver disease and polycystic ovary syndrome
- Genomic and phenotypic characterization of Investigator Global Assessment (IGA) scale-based endotypes in atopic dermatitis
- Gene-Environment Interaction Between <i>CYP1B1</i> and Oral Contraception on Frontal Fibrosing Alopecia
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Acquired progressive kinking of the hair in a prepubertal boy