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Research 91–120 of 1000+
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- MendelVar: gene prioritization at GWAS loci using phenotypic enrichment of Mendelian disease genes
- Heterozygous deletion of the <i>NSDHL</i> gene in an Appenzeller Mountain Dog with verrucous epidermal keratinocytic nevi
- Increased DHT levels in androgenic alopecia have been selected for to protect men from prostate cancer
- Prevalence of rs1998076 and Its Association with Androgenetic Alopecia in Indonesian Population: A Pilot Study
- Deletion of an enhancer in FGF5 is associated with ectopic expression in goat hair follicles and the cashmere growth phenotype
- GWAS Identifies Three Susceptibility Loci for Trichilemmal Cysts
- Gene Variant in Amish a Clue to Better Aging
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Characterisation of Ovine KRTAP19-3 and Its Impact on Wool Traits in Chinese Tan Sheep
- 481 Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Deciphering the pathogenesis of central centrifugal cicatricial alopecia
- 284 Deciphering the pathogenesis of central centrifugal cicatricial alopecia
- Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition
- Several variants on chromosome 10 are associated with coarse hair diameter in Dazu black goats (<i>Capra hircus</i>)
- Woolly hair generalizado: caso clínico e revisão da literatura
- Genes of Congenital Dermatologic Disorders in Dogs—A Review
- Identification of a recurrent nonsense mutation in <i>HR</i> gene responsible for atrichia with papular lesions in two Kashmiri families
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Genetic variation in the ovine <i>KAP22-1</i> gene and its effect on wool traits in Egyptian sheep
- The role of candidate pharmacogenetic variants in determining valproic acid efficacy, toxicity and concentrations in patients with epilepsy
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- THERAPEUTIC HOTLINE: Genetic variations in the androgen receptor gene and finasteride response in women with androgenetic alopecia mediated by epigenetics
- Complex genetic dependencies among growth and neurological phenotypes in healthy children: Towards deciphering developmental mechanisms