Evidence for Genetic Heterogeneity in X-Linked Congenital Stationary Night Blindness
- 1 April 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 62 (4) , 865-875
- https://doi.org/10.1086/301781
Abstract
No abstract availableKeywords
This publication has 43 references indexed in Scilit:
- Integration of 101 DNA markers across human Xp11 using a panel of somatic cell hybridsCytogenetic and Genome Research, 1997
- The 1993–94 Généthon human genetic linkage mapNature Genetics, 1994
- Integrated human genome–wide maps constructed using the CEPH reference panelNature Genetics, 1994
- Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage mapNature Genetics, 1994
- Rhodopsin mutation G90D and a molecular mechanism for congenital night blindnessNature, 1994
- Additional Evidence for a Gene Locus for Progressive Cone Dystrophy with Late Rod Involvement in Xp21.1-p11.3Genomics, 1993
- Linkage analysis in X-linked congenital stationary night blindnessGenomics, 1992
- Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7Genomics, 1992
- Åland eye disease: Linkage dataGenomics, 1991
- Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3Genomics, 1989