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Research 121–150 of 1000+
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- 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
- Monilethrix: A rare hereditary condition
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Clinical and Genetic Characterization of Tunisian Children with Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- 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
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Marie‐Unna Hereditary Hypotrichosis or Autosomal Recessive Hereditary Hypotrichosis with Woolly Hair: The Diagnostic Dilemma of Labeling Cases with Hypotrichosis
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Treatments of hereditary hair loss (alopecia)
- Congenital and Hereditary Skin Diseases
- Congenital and Hereditary Skin Diseases
- Quantitative image analysis for hereditary hair disorders
- Emergence of hereditary hyperplastic gingivitis in Newfoundland and Labrador, Canada: an exploration into the molecular aetiology at both the gene and genome levels
- Case Study: Hereditary Cancer Genetic Testing in Unaffected Patients May Allow for Early Intervention and Aggressive Management
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Dyschromatosis Universalis Hereditaria: Report of a case and Review of the Literature
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- 6874 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- SUN-332 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- Clinical and molecular genetic studies in hereditary hair loss
- IMMUNOLOGICAL AND GENETIC ASPECTS OF HEREDITARY ANTIBODY DEFICIENCIES