Three-point linkage analysis using multiple DNA polymorphic markers in families with X-linked nephrogenic diabetes insipidus
- 1 April 1989
- Vol. 4 (3), 434-437
- https://doi.org/10.1016/0888-7543(89)90352-2
Abstract
No abstract availableThis publication has 22 references indexed in Scilit:
- Localization of the gene for X-linked nephrogenic diabetes insipidus to Xq28American Journal of Medical Genetics, 1988
- Linkage of X-Linked Nephrogenic Diabetes insipidus with DXS52, a Polymorphic DNA MarkerNephron, 1988
- Deletion of the DXS165 locus in patients with classical ChoroideremiaClinical Genetics, 1987
- Linkage of adrenoleukodystrophy to a polymorphic DNA probeAnnals of Neurology, 1987
- RFLP FOR LINKAGE ANALYSIS OF FRAGILE X SYNDROMEThe Lancet, 1987
- Application of three intragenic DNA polymorphisms for carrier detection in haemophilia B.Journal of Medical Genetics, 1986
- Use of a BamHI polymorphism in the factor IX gene for the determination of hemophilia B carrier statusBlood, 1986
- Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie diseaseCytogenetic and Genome Research, 1986
- The Genetic Linkage Map of the Human X ChromosomeScience, 1985
- Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII geneNature, 1985