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Research 211–240 of 1000+
- Gomez?Lopez?Hernandez syndrome: another consideration in focal congenital alopecia
- CYP21A2 Genotypes do not Predict the Severity of Hyperandrogenic Manifestations in the Nonclassical Form of Congenital Adrenal Hyperplasia
- Sexual Function and Depressive Symptoms in Young Women With Nonclassic Congenital Adrenal Hyperplasia
- Poikiloderma congenitale-an early case of rothmund-thomson's syndrome.
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Nonclassic congenital adrenal hyperplasia and the heterozygote carrier
- PSAT097 Patient Preference Research: Preferred Adjunctive Medication Attributes of Adult Patients with Classic Congenital Adrenal Hyperplasia
- Diffuse congenital hypotrichosis simplex with associated hair shaft fragility
- 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
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Giant Congenital Melanocytic Nevus Correction: A Case Report
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Nonclassic Congenital Adrenal Hyperplasia: An Overview
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Pachyonychia Congenita-Associated Alopecia. A Microscopic Analysis Using Transverse Section Technique
- A new type of pachyonychia congenita.
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Resolution of the plantar hyperkeratosis of pachyonychia congenita during chemotherapy for Ewing sarcoma
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay
- Hypotrichosis congenita of Marie Unna
- Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency revisited: an update with a special focus on adolescent and adult women
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Non-classic congenital adrenal hyperplasia
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I