Linkage to Xq28 in a family with nonspecific X-linked mental retardation
Open Access
- 1 November 1992
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 90 (3), 263-266
- https://doi.org/10.1007/bf00220075
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Localisation of the MRX3 gene for non-specific X linked mental retardation.Journal of Medical Genetics, 1991
- Genetic mapping of new RFLPs at Xq27–q28Genomics, 1991
- Assignment of X-linked hydrocephalus to Xq28 by linkage analysisGenomics, 1990
- MASA syndrome: further clinical delineation and chromosomal localisationHuman Genetics, 1989
- Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromesGenomics, 1989
- Improved DNA markers for efficient analysis of fragile X familiesAmerican Journal of Medical Genetics, 1988
- Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qterHuman Genetics, 1987
- Linkage studies of X-linked recessive spastic paraplegia using DNA probesHuman Genetics, 1986
- On the gates of hell and a most unusual geneAmerican Journal of Medical Genetics, 1986
- A CLINICALLY USEFUL DNA PROBE CLOSELY LINKED TO HAEMOPHILIA AThe Lancet, 1984