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- Characteristics of phenotypes (clinical variants) of polycystic ovary syndrome in women of reproductive age
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- 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
- TREATMENT OF KERATOSIS PILARIS: A NARRATIVE LITERATURE REVIEW OF TOPICAL, PROCEDURAL, AND VARIANT-SPECIFIC THERAPIES
- Lichen planopilaris epidemiology: a retrospective study of 80 cases
- The diagnosis of polycystic ovary syndrome in adolescents
- Cell Polarization Defects in Early Heart Development
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- INTERFERONS IN DERMATOLOGY
- Evaluating combined therapy with myoinositol and D-chiro-inositol in infertility management across PCOS phenotypes: a comprehensive retrospective data analysis
- Cardiovascular and Metabolic Risk Profiles Across Different Phenotypes of Polycystic Ovary Syndrome
- Timing of expression of the core clock gene <i>Bmal1</i> influences its effects on aging and survival
- Predicting Human Appearance from DNA for Forensic Investigations
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- Spectrum of Phenotypes Associated with Human MC1R Variations
- CUTANEOUS T-CELL LYMPHOMA
- Muscle pain in a woman with congenital adrenal hyperplasia due to 21-hydroxylase deficiency resolved with testosterone therapy. A case report with 10 years of follow-up
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- current possible treatment approaches of Polycystic Ovary Syndrome (PCOS)
- 0952 Spatial transcriptomics reveal compartmentalized dysregulation of lipid metabolism in acne vulgaris
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Exogenous calreticulin improves diabetic wound healing
- Prevalence and Metabolic Characterization of Polycystic Ovary Syndrome in a Cohort of Patients Diagnosed with Spina Bifida: Study Protocol
- A Comprehensive Approach in Diagnosing the Polycystic Ovary Syndrome
- Polycystic Ovary Syndrome
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome