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Research 331–360 of 1000+
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Alopecia in a 19-Month-Old Boy
- Distancia promedio de la línea de implantación pilosa frontal y sus estructuras en una población de mujeres colombianas
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Genetic correlation by pedigree analysis in patients diagnosed with PCOS as per Rotterdam’s criteria
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Fibrosing Frontal Alopecia: A comprehensive study to understand its etiology
- Androgenetic alopecia: An autosomal dominant disorder
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Monilethrix: A rare hereditary condition
- P378: Expanding the phenotype of hyper-IgE syndrome: Heterozygous VUS in IL6ST with elevated serum IgE and isolated abscesses
- Monilethrix in three generations
- Marie-unna hereditary hypotrichosis
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Monilethrix – Case report of a rare disease
- A retrospective study on the characteristics of androgenetic alopecia among Asian races in the National Skin Centre, a tertiary dermatological referral centre in Singapore.
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- The inheritance of common baldness: Two B or not two B ?
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome