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Research 721–750 of 1000+
- S3507 GI Bleed Leading to Discovery of Hereditary Hemochromatosis
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- [Monilethrix is a hereditary hair shaft disorder].
- Hereditary, Congenital, and Acquired Alopecias
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature
- Hereditary, Congenital, and Acquired Alopecias
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Successful treatment of hereditary hypotrichosis simplex by platelet rich plasma injection with topical minoxidil 2%
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Hereditary Androgenetic Alopecia and Minoxidil
- Keratoma Hereditaria Mutilans (Vohwinkel's Disease) with Congenital Alopecia Universalis (Atrichia Congenita)
- [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
- Topical Minoxidil Therapy in Hereditary Androgenetic Alopecia
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- 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
- 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
- Treatments of hereditary hair loss (alopecia)
- Congenital and Hereditary Skin Diseases