Search
for
Sort by
Research 181–210 of 1000+
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- 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
- 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
- Hereditary, Congenital, and Acquired Alopecias
- Hereditary, Congenital, and Acquired Alopecias
- Molecular Basis of Hereditary Hair Diseases
- Congenital and Hereditary Skin Diseases
- Clinical and molecular genetic studies in hereditary hair loss
- Coat Problems
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Monilethrix: Beaded hair and hypotrichosis in a child
- BG01 Confirming small nuclear ribonucleoprotein polypeptide E as a cause of nonsyndromic hypotrichosis
- Pathology in Practice
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix
- Autosomal recessive woolly hair/hypotrichosis with homozygous mutation in the <i>LIPH</i> gene: a case report
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Ectodermal Dysplasia: Variable Expressions
- A rare hair loss in children: Monilethrix
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- [Hirsutism].