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Research 271–300 of 1000+
- Forensic approach in cases of anabolic-androgenic steroid abuse and cardiovascular mortality: insights from autopsy, histopathology, immunohistochemistry and toxicology
- Adrenal and Gonadal Activity, Androgen Concentrations, and Adult Height Outcomes in Boys With Silver-Russell Syndrome
- Werner's syndrome: incidental finding during pregnancy
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- P448: Identification of a novel RPS6KA3 variant in a female child with features of Coffin-Lowry syndrome: A case study
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Trichothiodystrophy in a child with occult learning disorder
- Mice lacking the epidermal retinol dehydrogenases SDR16C5 and SDR16C6 display accelerated hair growth and enlarged meibomian glands
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Abordagens psicológicas e novas terapêuticas perante as escolhas do paciente portador da Síndrome de Morris
- Polycystic ovary syndrome and its management: In view of oxidative stress
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- The first case report of kerion-type scalp mycosis caused by Aspergillus protuberus
- Polycystic Ovary Syndrome: It’s Not Just Infertility
- The Role of the Athletic Trainer in Providing Care to Transgender and Gender-Diverse Patients: Considerations for Medical Affirmation—Part II
- Transgender Competent Provider
- Congenital insensitivity to pain with anhidrosis and progressing acro-osteolysis: a case report with 7-year follow-up
- Trichothiodystrophy
- Incel Identity Development: A Scoping Review of Biopsychosocial Markers
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- TONGUE, RED
- Recent advances in Forensic DNA Phenotyping of appearance, ancestry and age
- Anatomical, physiological, and behavioral mechanisms of thermoregulation in elephants
- Epigenetic regulation of 5α reductase-1 underlies adaptive plasticity of reproductive function and pubertal timing
- Testing the impact of trait prevalence priors in Bayesian-based genetic prediction modeling of human appearance traits
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models