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Research 811–840 of 1000+
- Genetics and Pathophysiology of Congenital Adrenal Hyperplasia
- 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
- [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
- S3507 GI Bleed Leading to Discovery of Hereditary Hemochromatosis
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Alopecia in a 19-Month-Old Boy
- Genetic correlation by pedigree analysis in patients diagnosed with PCOS as per Rotterdam’s criteria
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Monilethrix: A rare hereditary condition
- 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
- Tricorrexis nudosa localizada por aplicación compulsiva de minoxidil
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene