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Research 91–120 of 1000+
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Immunomodulators in the treatment of cutaneous lymphoma
- Identification of the Keratin-Associated Protein 22-2 Gene in the Capra hircus and Association of Its Variation with Cashmere Traits
- The hair shaft: normality, abnormality, and genetics
- Evidence-Based and Potential Benefits of Metformin in the Polycystic Ovary Syndrome: A Comprehensive Review
- COVID-19 and Sex Differences
- An Update of Congenital Adrenal Hyperplasia
- Male-pattern baldness susceptibility locus at 20p11
- A new path in defining light parameters for hair growth: Discovery and modulation of photoreceptors in human hair follicle
- Polycystic ovary syndrome and impact on health
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- How to diagnose a lipodystrophy syndrome
- SARS-CoV-2 Spike Protein S1-Mediated Endothelial Injury and Pro-Inflammatory State Is Amplified by Dihydrotestosterone and Prevented by Mineralocorticoid Antagonism
- Nonclassic Congenital Adrenal Hyperplasia
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer
- Current evaluation of amenorrhea
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Nonclassic congenital adrenal hyperplasia
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Clinical Significance of Dense Fine Speckled Pattern in Anti-nuclear Antibody Test using Indirect Immunofluorescence Method
- MicroRNA in skin diseases
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Congenital adrenal hyperplasia
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Human Adipose-Derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Recent Advances in Drug Design and Drug Discovery for Androgen- Dependent Diseases
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- Study on Changes of 19 Steroids in Plasma From 9 Diagnosed Patients With P450 Oxidoreductase Deficiency