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Research 421–450 of 1000+
- Acute Localised Exanthematous Pustulosis
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- Ehlers-Danlos syndrome: From bedside to bench
- Androgen sensitivity gateway to COVID‐19 disease severity
- Pili trianguli et canaliculi as a phenotypic subtype in patients with central centrifugal cicatricial alopecia: A scanning electron microscopy study
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Lack of concordance and linkage disequilibrium among brothers for androgenetic alopecia and CAG/GGC haplotypes of the androgen receptor gene in Mexican families
- KASUS RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA-MITIS YANG TERDIAGNOSIS PADA SAAT LANJUT USIA
- Obesity and Polycystic Ovary Syndrome: Implications for Pathogenesis and Novel Management Strategies
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- 8507 Misdiagnosis of Graves’ and RAI Treatment in Patient with THRB Gene Mutation
- News in brief
- Development, Regeneration, and Evolution of Feathers
- The Double Edge Sword of Testosterone’s Role in the COVID-19 Pandemic
- Polycystic ovary syndrome in adult women
- Clinical Manifestations of Hyperandrogenism and Ovulatory Dysfunction Are Not Associated with His1058 C/T SNP (rs1799817) Polymorphism of Insulin Receptor Gene Tyrosine Kinase Domain in Kashmiri Women with PCOS
- Clinical Snippets
- Identification and sequence analysis of the keratin-associated protein 24‐1 (KAP24-1) gene homologue in sheep
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Ottawa, Ontario, Canada, February 13–16, 2013
- 5α Reductase Deficiency—a Rare Cause of Ambiguous Genitalia and Gender Dysphoria
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Clinical features of non‐classical 21‐hydroxylase deficiency after normal newborn mass screening
- HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome
- Prostate cancer and androgenic alopecia
- Biotin and Acetazolamide for Treatment of an Unusual Child With Autism Plus Lack of Nail and Hair Growth
- 46, XY 5-Alpha Reductase Deficiency in a 36-Year-Old Phenotypic Female Patient
- Whole-genome sequencing of eight goat populations for the detection of selection signatures underlying production and adaptive traits