Three DNA markers for hypophosphataemic rickets
- 1 July 1992
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 89 (5) , 539-542
- https://doi.org/10.1007/bf00219180
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- Genetic mapping of 12 marker loci in the Xp22.3-p21.2 regionHuman Genetics, 1991
- Refined localization of the gene causing X-linked juvenile retinoschisisGenomics, 1991
- Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets familiesGenomics, 1990
- The human glycine receptor: A new probe that is linked to the X-linked hypophosphatemic rickets geneGenomics, 1990
- Parabiosis suggests a humoral factor is involved in X-linked hypophosphatemia in miceJournal of Bone and Mineral Research, 1989
- Report of the committee on the genetic constitution of the X chromosome (Part 1 of 3)Cytogenetic and Genome Research, 1989
- DNA linkage analysis of X-linked retinoschisisHuman Genetics, 1988
- Bridging markers defining the map position of X linked hypophosphataemic rickets.Journal of Medical Genetics, 1987
- Evidence for an Intrinsic Renal Tubular Defect in Mice with Genetic Hypophosphatemic RicketsJournal of Clinical Investigation, 1979
- Renal handling of phosphate in vivo and in vitro by the X-linked hypophosphatemic male mouse: Evidence for a defect in the brush border membraneKidney International, 1978