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Research 361–390 of 1000+
- Bamboo Hair Syndrome or Netherton Syndrome - A Case Report
- Emergence of hereditary hyperplastic gingivitis in Newfoundland and Labrador, Canada: an exploration into the molecular aetiology at both the gene and genome levels
- Management of pregnancy in a carrier of the Donohue mutation
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- Lanceolate hair-J (<i>lah<sup>J</sup> </i> ): A mouse model for human hair disorders
- Primary and Secondary Disturbances in Trace Element Metabolism Connected with Genetic Metabolic Disorders
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- [Dermatophytic disease: exuberant hyperkeratosis with cutaneous horns].
- 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
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Reviewer #2 (Public Review): CaBP1 and 2 enable sustained CaV1.3 calcium currents and synaptic transmission in inner hair cells
- 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
- Clinical Snippets
- Clinical Snippets
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- 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
- 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