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Research 511–540 of 1000+
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Aplasia cutis congenita on lumbosacral area
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Congenital atrichia with papular lesions
- Cutaneous Mastocytosis Associated With Congenital Alopecia
- Congenital Hypotrichosis in a White-Tailed Deer Fawn from South Dakota
- Giant Congenital Blue Nevus Presenting as Cutis Verticis Gyrata: A Case Report and Review of the Literature
- A Case of Congenital Alopecia Areata Successfully Diagnosed by Integrating Clinical, Trichoscopic, and Scalp Biopsy Findings
- Congenital Hypotrichosis in a White-Tailed Deer Fawn from
- <i>In vivo</i> alteration of the keratin 17 gene in hair follicles by oligonucleotide‐directed gene targeting
- Pachyonychia congenita: Sporadic onset with mutation analysis
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- Congenital adrenal hyperplasia
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Keratoma Hereditaria Mutilans (Vohwinkel's Disease) with Congenital Alopecia Universalis (Atrichia Congenita)
- Congenital triangular alopecia: A close mimicker of alopecia areata
- Early Diffuse Alopecia in a Neonate with Congenital Syphilis
- Congenital atrichia with papular lesions
- Congenital hypotrichosis in a French bulldog
- Improvement of Skin Lesions in an Adult with CHILD Syndrome Treated with 2% Ketoconazole Cream
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- 301 The Spectrum of PLEC Sequence Variants and Related Plectinopathies Including Novel Association with Epidermolysis Bullosa Pruriginosa
- Immunological control of skin development: from homeostasis to developmental pathologies
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- 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
- 321 Deletion of hypoxia-inducible factor prolyl 4-hydroxylase 2 in FoxD1-lineage mesenchymal cells leads to congenital truncal alopecia
- Dermatologic Disorders