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Research 61–90 of 522
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Mosaic Hair Regrowth Pattern of Ophiasis and Androgenic Alopecia in a Patient With Alopecia Areata Totalis
- Isochromosome Mosaic Turner Syndrome: A Case Report
- A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- PA15 Becker naevus syndrome associated with a mosaic pathogenic variant in <i>ACTB</i>
- SUN-208 Rare Case of 47XXY/46XX Mosaic Klinefelter Syndrome
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- A Clinical Genetics-Driven Dual Diagnosis of Prader–Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL
- Genetic Fate Mapping Using Site-Specific Recombinases
- Double-Lined Frontoparietal Scleroderma en coup de sabre
- Epidermal field carcinogenesis in bald-headed: An attempt at finetuning early non-invasive detection
- Effect of gamma-ray exposure on the genome-editing efficiency of improved genome-editing via oviductal nucleic acids delivery (<i>i</i>-GONAD)
- Phylloid terminal hair nevus: A unique clinical entity
- Temporal triangular alopecia and a review of 52 past cases
- Loss of the Y Chromosome: A Review of Molecular Mechanisms, Age Inference, and Implications for Men’s Health
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis
- Treatment-resistant Schizophrenia and Global Cortical Atrophy in a Patient with Turner Syndrome
- Injury suppresses Ras cell competitive advantage through enhanced wild-type cell proliferation
- Clinical Snippets
- Minoxidil-induced lung disease, masquerading as hypersensitivity pneumonitis
- A case of 21-hydroxylase deficiency in Turner′s syndrome and literature review
- Hemidesmosomes and Notch signaling regulate epidermal differentiation via delamination
- Epithelial stem cells and implications for wound repair
- Renbök Phenomenon in a Patient With Alopecia Areata Universalis
- Nevus psiloliparus: Newly described histopathological features from transverse sections
- Trends in Human Hair Growth and Alopecia Research
- Acne Syndromes and Mosaicism
- Pallister-Killian Syndrome