The Genetics of Ichthyosis: A Primer for Epidemiologists.
- 1 June 1994
- journal article
- review article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 102 (6) , 49S-50S
- https://doi.org/10.1111/1523-1747.ep12388591
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Genetic skin diseases caused by mutations in keratin intermediate filamentsTrends in Genetics, 1993
- Linkage of the Epidermolytic Hyperkeratosis Phenotype and the Region of the Type II Keratin Gene Cluster on Chromosome 12Journal of Investigative Dermatology, 1992
- Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12qNature Genetics, 1992
- Prenatal diagnosis of congenital non‐bullous ichthyosiform erythroderma (lamellar ichthyosis)Prenatal Diagnosis, 1987
- Steroid sulphatase deficiency diseaseClinical Genetics, 1985
- Antenatal diagnosis of steroid sulphatase deficiency: case report and literature survey.Journal of Clinical Pathology, 1982
- Prenatal Diagnosis of Congenital Bullous Ichthyosiform Erythroderma (Epidermolytic Hyperkeratosis) by Fetal Skin BiopsyNew England Journal of Medicine, 1980
- Ichthyosiform DermatosesJournal of Investigative Dermatology, 1973
- Clinical Features of Autosomal Dominant and Sex-linked Ichthyosis in an English PopulationBMJ, 1966
- Genetic classification of ichthyosisArchives of Dermatology, 1965