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Research 61–90 of 1000+
- Mini Review on Polycystic Ovary Syndrome (PCOS)
- Low-dose oral minoxidil in a case of short anagen syndrome
- Cutaneous lupus erythematosus
- Transcriptomic regulation of seasonal coat color change in hares
- Polycystic ovary syndrome in adolescents
- Integration of Ethylene and Auxin Signaling and the Developmental Consequences of Their Crosstalk
- Delayed Diagnosis of Familial Adenomatous Polyposis-related Colon Cancer in an Adolescent with Coexisting Eating Disorder: A Case Report
- EP1725 - LBA_ECE_1089 - A wolf in sheep's clothing: unmasking CAH in a “PCOS” patient with co-occurring POTS and Ehlers-Danlos syndrome
- Copy number variation regions in Nellore cattle: Evidences of environment adaptation
- Genetic basis of polycystic ovary syndrome
- A Practitioner's Guide to Hair Loss Part 1—History, Biology, Genetics, Prevention, Conventional Treatments, and Herbals
- Genetic prediction of male pattern baldness
- What does acne genetics teach us about disease pathogenesis?
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Genetic Fate Mapping Using Site-Specific Recombinases
- Molecular Genetics of Alopecias
- Genetic determinants of skin ageing: a systematic review and meta-analysis of genome-wide association studies and candidate genes
- SNP Markers: Analysis of Genetic Diversity and Identification of Genomic Regions in Pantaneiro Sheep and Texel Sheep Under Natural Selection
- Genetic Defects of Female Sexual Differentiation
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Molecular genetics of androgen insensitivity
- Polarized microscopy in genetic hair disorders: case series
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Potential genetic associations of acne scar phenotypes: IL1A in fibrotic scarring and CYB5R1 in atrophic scarring
- Biology and Genetics of Hair
- Considerations in genetic counseling of transgender patients: Cultural competencies and altered disease risk profiles