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Research 30 of 499
- Phylloid terminal hair nevus: A unique clinical entity
- Analogs of human genetic skin disease in domesticated animals
- TRANSMEDCON 2022: E-Poster Abstracts
- Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- Acne Syndromes and Mosaicism
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Molecular pathology of skin adnexal tumours
- Stem Cell Competition for Niche Occupancy: Emerging Themes and Mechanisms
- Hirsutism in the Adolescent Female
- Atlas of Geriatric Dermatology
- Genetic Defects of Female Sexual Differentiation
- Pigmentary mosaicism: An update
- Dermatoscopy of hair shaft disorders
- Poster Presentations
- Hair shaft disorders in children – An update
- Congenital Trichomegaly of the Eyelashes
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- The Genetics of Human Skin Disease
- Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Association of Acne Tarda with Endocrinological Disorders
- Focused Review on Metal Nanoparticles in Hair Regeneration and Alopecia: Insights into Mechanisms, Assessment Techniques, Toxicity, Regulatory and Intellectual Property Perspectives
- Role of polymorphism of the androgen receptor gene and non-random X chromosome inactivation in the genesis of androgenic alopecia in women of childbearing potential
- Generating mouse models of degenerative diseases using Cre/lox-mediated in vivo mosaic cell ablation
- Alopecia areata and relapsing polychondritis or mosaic autoimmunity? The first experience of co-trimoxazole treatment
- 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