Genetic mapping of Xp22.12–p22.31, with a refined localization for spondyloepiphyseal dysplasia (SEDL)
- 1 October 1995
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 96 (4) , 407-410
- https://doi.org/10.1007/bf00191797
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Fine deletion mapping of the p22 region of the human X chromosome using a radiation-induced hybrid panelCytogenetic and Genome Research, 1995
- The 1993–94 Généthon human genetic linkage mapNature Genetics, 1994
- Hypomagensemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpointHuman Genetics, 1994
- Report of the Fifth International Workshop on Human X Chromosome Mapping 1994 (Part 1 of 4)Cytogenetic and Genome Research, 1994
- The Gene for Spondyloepiphyseal Dysplasia (SEDL) Maps to Xp22 between DXS16 and DXS92Genomics, 1993
- Directed isolation of human genes that escape X inactivationSomatic Cell and Molecular Genetics, 1992
- Spondyloepiphyseal dysplasia tarda: linkage with genetic markers from the distal short arm of the X chromosomeHuman Genetics, 1988
- Strategies for multilocus linkage analysis in humans.Proceedings of the National Academy of Sciences, 1984
- Spondyloepiphyseal dysplasia tarda: a report of four cases in two familiesThe British Journal of Radiology, 1973