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Research 31–60 of 1000+
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6
- Recurrent E413K Mutation of hHb6 in a Japanese Family with Monilethrix
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Missense mutation Y449H of the K10 gene in a patient with severe epidermolytic ichthyosis
- Two females with hair loss
- Informàtica i Dret penal: Els delictes relatius a la informàtica
- Clinical and molecular genetic studies in hereditary hair loss
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene
- Porphyria Cutanea Tarda in a Patient With Agnogenic Myeloid Metaplasia
- Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis
- A University Center for the Performing Arts
- Alopezien und Hypotrichosen im Kindesalter
- Alopecia in a 19-Month-Old Boy
- Monilethrix with Acitretin
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- PSEUDOPELADE: AN INHERITED ALOPECIA
- Acquired Uncombable Hair
- A retrospective study on the characteristics of androgenetic alopecia among Asian races in the National Skin Centre, a tertiary dermatological referral centre in Singapore.
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation