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Genomic imprinting: support for the concept from a study of Prader-Willi Syndrome patients
In this study, nineteen cases of suspected or clinically diagnosed Prader-Willi Syndrome (PWS) were tested for molecular deletions by in situ hybridization with two DNA probes, IR4-3R and GABRB3. Both probes are specific for sequences within the chromosome region 15q11-13, with IR4-3R located within the putative PWS region and GABRB3 in the distal area associated with Angelman Syndrome.
Date:
December 1994
Creator:
Robinett, Sheldon J. (Sheldon Jay)
System:
The UNT Digital Library