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Research 691–720 of 1000+
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Primary and Secondary Disturbances in Trace Element Metabolism Connected with Genetic Metabolic Disorders
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Deep facial mycosis due to <i>Trichophyton verrucosum</i>—molecular genetic identification of the dermatophyte in paraffin‐embedded tissue—case report and review of the literature
- Clinical Management of Prostate Cancer in High-Risk Genetic Mutation Carriers
- A new familial presentation of dissecting cellulitis: The genetic implications on scarring alopecias
- Lipedematous Scalp Occurring in Two Female Siblings: Further Evidence for a Genetic Role
- GENOME-WIDE ANALYSIS REVEALS THE MOLECULAR BASIS OF GENETIC VARIATION OF IMPORTANT ECONOMIC TRAITS IN CASHMERE GOATS ON QINGHAI-TIBET PLATEAU
- A Review on Unraveling the Complexity of Autoimmune Skin Disorders: Genetic Influences, Environmental Triggers and Innovative Management Approaches
- Tracking the Path of the Original: A Forensic Genetic, Demographic, and Legal Audit of the Muur Continuity Hypothesis
- Tracking the Path of the Original: A Forensic Genetic, Demographic, and Legal Audit of the Muur Continuity Hypothesis
- Epidemiology, Genetics & Risk factors in Alopecia Androgenetics
- Functional divergence of plant expansins as revealed by genetic complementation of root-hair tip growth in <i>Arabidopsis thaliana</i>
- P-055 MONOZYGOTIC TRANSGENDER MALE TWINS: A CASE REPORT HIGHLIGHTING GENETIC CONCORDANCE IN GENDER DYSPHORIA
- Björnstad Syndrome With Late‐Onset Alopecia Mimicking Androgenetic Alopecia: Histopathological and Genetic Findings
- Correction to “MiR‐200c‐3p as a Novel Genetic Marker and Therapeutic Tool for Alopecia Areata”
- BH26 First reported case of lichen planopilaris in siblings: evidence for a genetic link?
- 8368 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- 9209 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- Pharmacogenetic Determinants of Valproic Acid Efficacy, Toxicity, and Serum Levels in Genetic Generalized Epilepsy
- Integrated single-cell chromatin and transcriptomic analyses of human scalp reveal etiological insights into genetic risk for hair and skin disease
- BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations
- Meeting Report: 68th Montagna Symposium on the Biology of Skin “Decoding Complex Skin Diseases: Integrating Genetics, Genomics, and Disease Biology”
- PROCEEDİNGS OF THE FIRST INTERNATIONAL SCIENTIFIC PRACTICAL ONLINE CONFERENCE HUMAN GENETICS AND GENETIC DISEASES: PROBLEMS AND DEVELOPMENT PERSPECTIVES
- Part 1. Genetic pathway of maternal transmission in Topiramate-treated zebrafish modelPart 2.Effects of herbal medicine on zebrafish embryos
- The Successful Treatment of Alopecia Areata with Platelet Rich Plasma in a Case of Twins with Genetic Risk for Autoimmune Disorders
- Polycystic Ovary Syndrome: Conditions, Genetics and Current Cure
- Skin, Genetic Defects, and Aging
- 9. Immunology and Genetics
- Case report: a study of the clinical characteristics and genetic variants of post-finasteride syndrome patients