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Research 211–240 of 1000+
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Recently Identified Forms of Epidermolysis Bullosa
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- Current Genetics in Hair Diseases
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Case Report: Androgen-secreting pediatric adrenocortical tumor of uncertain malignant potential presenting with virilization in a 19-month-old girl
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Clinical Snippets
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Biologically Driven Innovations in Aesthetic Surgery: Advances in Regenerative and Cellular Therapies
- Keratin disorders: from gene to therapy
- Congenital Adrenal Hyperplasia
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Genetics and Pathophysiology of Congenital Adrenal Hyperplasia
- Improving human forensics through advances in genetics, genomics and molecular biology
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Werner′s syndrome
- Sarcoptic mange outbreak decimates South American wild camelid populations in San Guillermo National Park, Argentina
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Editors' Picks