Autosomal dominant retinitis pigmentosa: a new multi-allelic marker (D3S621) genetically linked to the disease locus (RP4)
- 1 March 1991
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 86 (5) , 502-504
- https://doi.org/10.1007/bf00194642
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- AUTOSOMAL DOMINANT RETINITIS-PIGMENTOSA - ABSENCE OF THE RHODOPSIN PROLINE-]HISTIDINE SUBSTITUTION (CODON 23) IN PEDIGREES FROM EUROPE1990
- A point mutation of the rhodopsin gene in one form of retinitis pigmentosaNature, 1990
- Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3Genomics, 1989
- AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA - EXCLUSION OF THE GENE FROM THE SHORT ARM OF CHROMOSOME-I INCLUDING THE REGION SURROUNDING THE RHESUS LOCUS1989
- A genetic linkage map of the human genomeCell, 1987
- Strategies for multilocus linkage analysis in humans.Proceedings of the National Academy of Sciences, 1984
- A novel repeated element with Z-DNA-forming potential is widely found in evolutionarily diverse eukaryotic genomes.Proceedings of the National Academy of Sciences, 1982
- POPULATION GENETIC-STUDIES OF RETINITIS PIGMENTOSA1980
- CONSTRUCTION OF A GENETIC-LINKAGE MAP IN MAN USING RESTRICTION FRAGMENT LENGTH POLYMORPHISMS1980
- Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.1974