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Research 31–60 of 1000+
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Fibrosing alopecia in a pattern distribution in two brothers with pili multigemini
- Polycystic ovarian syndrome: Prevalence and its correlates among adolescent girls
- Alopecia areata and Down syndrome: A true association and the importance of dermoscopic diagnosis
- Genetics of Diabetes in Childhood
- New developments in the molecular treatment of ichthyosis: review of the literature
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Genetic variants in androgenetic alopecia: insights from scalp RNA sequencing data
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1
- Estudo da diversidade dos genes MC1R e SLC24A5 em populações globais: avaliação de aspectos evolutivos e ambientais
- The analysis of genetics and associated autoimmune diseases in Chinese vitiligo patients
- No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- The quantification of reproductive hormones in the hair of captive adult brown bears and their application as indicators of sex and reproductive state
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Genome-based analysis of the genetic pattern of black sheep in Qira sheep
- Novel <i>RNF113A</i> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
- Disorders linked to insufficient androgen action in male children
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Racial variations in COVID‐19 deaths may be due to androgen receptor genetic variants associated with prostate cancer and androgenetic alopecia. Are anti‐androgens a potential treatment for COVID‐19?
- Role of cholesterol sulfate in epidermal structure and function: Lessons from X-linked ichthyosis
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Pediatric Features of Genetic Predisposition to Polycystic Ovary Syndrome
- Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay