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Research 781–810 of 1000+
- Erythromelanosis follicularis faciei et colli with reticulated hyperpigmentation of the extremities
- [Netherton's syndrome in two sisters].
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Reviewer #2 (Public Review): CaBP1 and 2 enable sustained CaV1.3 calcium currents and synaptic transmission in inner hair cells
- BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations
- S3507 GI Bleed Leading to Discovery of Hereditary Hemochromatosis
- Clinical Snippets
- Clinical Snippets
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- 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
- Genetic correlation by pedigree analysis in patients diagnosed with PCOS as per Rotterdam’s criteria
- Fibrosing Frontal Alopecia: A comprehensive study to understand its etiology
- 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
- P378: Expanding the phenotype of hyper-IgE syndrome: Heterozygous VUS in IL6ST with elevated serum IgE and isolated abscesses
- Monilethrix in three generations
- 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 ?
- 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
- Tricorrexis nudosa localizada por aplicación compulsiva de minoxidil
- Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis
- Familial Frontal Fibrosing Alopecia