Linkage of Wiskott-Aldrich syndrome with three marker loci, DXS426, SYP and TFE3, which map to the Xp11.3?p11.22 region
- 1 January 1993
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 92 (3) , 250-253
- https://doi.org/10.1007/bf00244467
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Physical mapping of 60 DNA markers in the p21.1 → q21.3 region of the human X chromosomeGenomics, 1991
- The gene encoding human TFE3, a transcription factor that binds the immunoglobulin heavy-chain enhancer, maps to Xp11.22Genomics, 1991
- An 18-locus linkage map of the pericentromeric region of the human X chromosome: Genetic framework for mapping X-linked disordersGenomics, 1991
- Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22–Xp11.3Genomics, 1991
- Linkage relationships of the Wiskott-Aldrich syndrome to 10 loci in the pericentromeric region of the human X chromosomeGenomics, 1990
- CLOSE LINKAGE OF HYPERVARIABLE MARKER DXS255 TO DISEASE LOCUS OF WISKOTT-ALDRICH SYNDROMEThe Lancet, 1989
- Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markersGenomics, 1988
- THE SYNAPTONEMAL COMPLEX IN GENETIC SEGREGATIONAnnual Review of Genetics, 1984
- The Wiskott-Aldrich syndrome in the United States and Canada (1892–1979)The Journal of Pediatrics, 1980
- Sex-Linked Hereditary Thrombocytopenia with Immunological DefectsHuman Heredity, 1975