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- 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: Identification of a U2HR mutation in the family from the original 1925 report
- Marie-unna hereditary hypotrichosis
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature
- [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- 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
- Significant Hair Regrowth With 5% Topical Minoxidil in a Child With Marie Unna Hereditary Hypotrichosis Caused by a Recurrent <i>HRURF</i> Variant
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- 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 or Autosomal Recessive Hereditary Hypotrichosis with Woolly Hair: The Diagnostic Dilemma of Labeling Cases with Hypotrichosis
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Two females with hair loss
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Polarized microscopy in genetic hair disorders: case series
- Clinical and molecular genetic studies in hereditary hair loss
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Biology and Genetics of Hair
- Molecular Basis of Hereditary Hair Diseases
- 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
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- The stem cell quiescence and niche signaling is disturbed in the hair follicle of the hairpoor mouse, an MUHH model mouse
- Inherited Disorders of the Hair
- Current Genetics in Hair Diseases
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family