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Research 61–90 of 1000+
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Inherited Disorders of the Hair
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Dermoscopic Features of Pili Annulati: Features of PA
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- ST Premature Graying Hair in Seven Years Old Children
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
- A new type of pachyonychia congenita.
- Pearly Pinna Papules in a Young Female
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Monilethrix with Acitretin
- Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6
- PSEUDOPELADE: AN INHERITED ALOPECIA
- Disorders of pigmentation in infants and children
- Sparse Brittle Hair and Bilateral Temporal Alopecia in a Child
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- [Wooly hair syndrome. Clinical and microscopic study].
- Biochemical features of primary cells from a pediatric patient with a gain-of-function <i>ODC1</i> genetic mutation
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Buschke-Ollendorff syndrome