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Research 121–150 of 1000+
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- Genetic Defects of Female Sexual Differentiation
- Genetic prediction of male pattern baldness
- The Genetics of Human Skin Disease
- Epigenetic age estimation in saliva and in buccal cells
- Genetic links between atopy, allergy, and alopecia areata: insights from a Mendelian randomization study
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- Genetics of thyroid lesions updated
- Genetic, hormonal and metabolic aspects of PCOS: an update
- What does acne genetics teach us about disease pathogenesis?
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- Genetic Fate Mapping Using Site-Specific Recombinases
- Genetic basis of polycystic ovary syndrome
- Genetic Susceptibility to Alopecia
- Genetic determinants of skin ageing: a systematic review and meta-analysis of genome-wide association studies and candidate genes
- A Practitioner's Guide to Hair Loss Part 1—History, Biology, Genetics, Prevention, Conventional Treatments, and Herbals
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Genetic correlation by pedigree analysis in patients diagnosed with PCOS as per Rotterdam’s criteria
- Polarized microscopy in genetic hair disorders: case series
- THE GENETICS OF CYP GENE VARIANTS IN ASSOCIATION WITH POLYCYSTIC OVARY SYNDROME: A NARRATIVE REVIEW
- Genetic Single Nucleotide Polymorphisms of IL-16 and its Concentration of Patients Infected with Alopecia Areata in Diyala Province, Iraq
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- The genetic basis of dermatophytosis skin infection susceptibility
- Generic competition and pharma patent strategies - a sequel
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Considerations in genetic counseling of transgender patients: Cultural competencies and altered disease risk profiles
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Dermatopathology and molecular genetics
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)