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- A Study on the Pattern of Genetic Inheritance of Polycystic Ovarian Syndrome
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Androgenetic Alopecia in Men: An Update On Genetics
- A genetic electrophoretic variant of high-sulfur hair proteins for forensic hair comparisons. I. Characterization of variant high-sulfur proteins of human hair.
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- 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
- Art’s Work in the Age of Biotechnology: Shaping Our Genetic Futures
- The Role of rs6152 Allele and Non-Genetic Factors in Androgenetic Alopecia: A Pilot Study in the Indonesian Local Population
- Clinical, Hormonal, Behavioral, and Genetic Characteristics of Androgen Insensitivity Syndrome in a Brazilian Cohort: Five Novel Mutations in the Androgen Receptor Gene
- Central Centrifugal Cicatricial Alopecia: New Insights and a Call for Action
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- 4 Vitamin D resistance
- Alopecia frontal fibrosante: revisão bibliográfica dos aspectos gerais, fisiopatológicos, diagnósticos e do tratamento
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Polymorphisms in Genes Involved in Steroidogenesis in the Development of Severe Acne
- Alopecia Areata in a Pediatric Patient with Delayed Maternal Manifestation: A Case Report
- Przewidywanie cech wyglądu człowieka na podstawie markerów DNA do celów medyczno-sądowych i kryminalistycznych
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Androgenetic alopecia: Update on etiology
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Genetic correlation by pedigree analysis in patients diagnosed with PCOS as per Rotterdam’s criteria
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Ocular aspects in biotinidase deficiency Clinical and genetic original studies
- Inheritance-Specific Dysregulation of Th1- and Th17-Associated Cytokines in Alopecia Areata
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome