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Research 571–600 of 1000+
- Congenital alopecia areata: a systematic review
- PA31 Congenital alopecia areata: a systematic review
- Chemical Danger in Hair Keratin Care
- Clinical and molecular genetic studies in hereditary hair loss
- Analysis of hair loss in young adults- A clinical study
- Congenital and Hereditary Skin Diseases
- Congenital and Hereditary Skin Diseases
- Congenital Triangular Alopecia
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- A polarizing light microscopy can be an easy and reliable diagnostic tool of congenital keratinizing disorders including Netherton syndrome
- Hereditary, Congenital, and Acquired Alopecias
- Hair loss: An epidemiologic approach
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
- Congenital Hypotrichosis in a White-Tailed Deer Fawn from
- N02. Hair and Nails
- <i>In vivo</i> alteration of the keratin 17 gene in hair follicles by oligonucleotide‐directed gene targeting
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families
- Recommendations for treatment of nonclassic congenital adrenal hyperplasia (NCCAH): An update
- Nonclassic Congenital Adrenal Hyperplasia
- Poikiloderma congenitale-an early case of rothmund-thomson's syndrome.
- Roux-en-Y gastric bypass in the treatment of non-classic congenital adrenal hyperplasia due to 11-hydroxylase deficiency
- PSAT097 Patient Preference Research: Preferred Adjunctive Medication Attributes of Adult Patients with Classic Congenital Adrenal Hyperplasia
- A Neonate with Unexplained Hair Loss
- Hair loss in infancy and childhood
- 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
- Giant Congenital Melanocytic Nevus Correction: A Case Report
- ODP408 Elevated DHEAS and Acute Hair Loss in an Adult Male with Trichorhinophalangeal Syndrome Type 1: a Case of Male PCOS
- Keratins of the Human Hair Follicle
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.