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Research 121–150 of 273
- A Rare Case of Postmenopausal Hirsutism Associated With a Serous Cystadenofibroma of the Ovary
- An adolescent girl presenting with primary amenorrhea: A case report of complete androgen insensitivity syndrome
- Iatrogenic Cushing's Syndrome in a Patient With Salt-Wasting Congenital Adrenal Hyperplasia (SWCAH)
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Treatment of Alopecia Universalis in a Child with Down Syndrome
- Development of Heritable Melanoma in Transgenic Mice
- Epithelial-to-Mesenchymal Stem Cell Transition in a Human Organ: Lessons from Lichen Planopilaris
- Current evaluation of amenorrhea
- An Interesting Case of Hepatic Adrenocortical Carcinoma.
- Measuring steroids in hair opens up possibilities to identify congenital adrenal hyperplasia in developing countries
- Unusual Presentation of Denys-Drash Syndrome in a Girl with Undisclosed Consumption of Biotin
- Treatment-resistant Schizophrenia and Global Cortical Atrophy in a Patient with Turner Syndrome
- Dermatologic care of patients with differences of sex development
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- Hirsutism-A Comprehensive Update of Embryology, Aetiopathogenesis and Therapeutic Approach
- Shallot (Allium ascalonicum): An overview of antidiabetic activity by α-glucosidase inhibition
- Polycystic Ovary Syndrome (PCOS) Presenting with Delayed Menarche and Clitoromegaly
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- A RARE CASE OF ISOLATED PULMONARY INVOLVEMENT IN LYMPHOID VARIANT HYPEREOSINOPHILIC SYNDROME
- Trichothiodystrophy in a child with occult learning disorder
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- P-055 MONOZYGOTIC TRANSGENDER MALE TWINS: A CASE REPORT HIGHLIGHTING GENETIC CONCORDANCE IN GENDER DYSPHORIA
- Wokeness in Our Practice
- Cross-sex hormone therapy for gender dysphoria
- Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes
- Overlap Between Ulerythema Ophryogenes and Keratosis Follicularis Spinulosa Decalvans: a Case Report
- Two parietal cephaloceles in a female neonate
- Long-term renewal of hair follicles from clonogenic multipotent stem cells
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder