Article
The Wiskott-Aldrich syndrome: refinement of the localization on Xp and identification of another closely linked marker locus, OATL1.
Human genetics - 1 Feb 1992
Greer W L, Peacocke M, Siminovitch K A
Abstract excerpt
The Wiskott-Aldrich syndrome (WAS) has previously been mapped to the proximal short arm of the X chromosome between the DXS14 and DXS7 loci. In this study, further segregation analysis has been performed using a newly identified WAS family as well as an additional marker probe, HOATL1. The result...
Topics
- Alleles
- Chromosome Mapping
- DNA
- Female
- Genetic Linkage
- Genetic Markers
- Humans
- Male
- Pedigree
- Polymorphism, Restriction Fragment Length
- Wiskott-Aldrich Syndrome
- X Chromosome
