Epidermolysis bullosa: Evidence for linkage to genetic markers on chromosome 1 in a family with the autosomal dominant simplex form
- 1 July 1990
- Vol. 7 (3) , 377-381
- https://doi.org/10.1016/0888-7543(90)90171-p
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3Genomics, 1989
- Twenty-eight loci form a continuous linkage map of markers for human chromosome 1Genomics, 1989
- A computer program to make linkage analysis with liped and linkage easier to perform and less prone to input errorsAnnals of Human Genetics, 1988
- A genetic linkage map of the human genomeCell, 1987
- Heterogeneity in the map distance between X-linked agammaglobulinemia and a map of nine RFLP lociHuman Genetics, 1986
- Genetic linkage analysis of epidermolysis bullosa simplex, Köbner typeAmerican Journal of Medical Genetics, 1984
- Characterization of an unusual DNA length polymorphism 5' to the human antithrombin III geneNucleic Acids Research, 1983
- GPT – Epidermolysis Bullosa Simplex (EBS Ogna) Linkage in ManHuman Heredity, 1973
- Epidermolysis bullosa.Journal of Medical Genetics, 1965