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Research 721–750 of 1000+
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Localized Autosomal Recessive Hypotrichosis Due to a Frameshift Mutation in the Desmoglein 4 Gene Exhibits Extensive Phenotypic Variability within a Pakistani Family
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis
- A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie‐Unna Hereditary Hypotrichosis or Autosomal Recessive Hereditary Hypotrichosis with Woolly Hair: The Diagnostic Dilemma of Labeling Cases with Hypotrichosis
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Topical fluocinolone acetonide acetate ointment in autosomal dominant congenital hypotrichosis
- Causes and Management of Hypertrichosis
- Coexistence of acquired localized hypertrichosis and lipoatrophy after lupus panniculitis
- Acquired Localized Hypertrichosis Following Pressure Garment and/or Silicone Therapy in Burn Patients
- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- Familial congenital generalized hypertrichosis
- Localized Acquired Hypertrichosis After Long-Term Repeated Cupping Therapy: A Case Report
- Localized acquired hypertrichosis on a miner’s shoulder: case report
- From rare hypertrichosis to common alopecia: new pathways for hair regeneration
- Acquired Localized Hypertrichosis Following Cast Application for Fracture
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- Diagnostic and therapeutic approaches for hypertrichosis
- DIFFERENT HORMONAL PATTERNS IN PREP'UBERTAL HYPERTRICHOSIS