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Research 331–360 of 1000+
- Alopecia totalis in an infant
- BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations
- S3507 GI Bleed Leading to Discovery of Hereditary Hemochromatosis
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- 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
- Distancia promedio de la línea de implantación pilosa frontal y sus estructuras en una población de mujeres colombianas
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- 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
- 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
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- P378: Expanding the phenotype of hyper-IgE syndrome: Heterozygous VUS in IL6ST with elevated serum IgE and isolated abscesses
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Marie-unna hereditary hypotrichosis
- 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
- Frontal Fibrosing Alopecia: A Review
- Tricorrexis nudosa localizada por aplicación compulsiva de minoxidil
- Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis
- Familial Frontal Fibrosing Alopecia
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Inherited Epidermolysis Bullosa: A Clinical Case