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.
| Identifer | oai:union.ndltd.org:unt.edu/info:ark/67531/metadc332745 |
| Date | 12 1900 |
| Creators | Robinett, Sheldon J. (Sheldon Jay) |
| Contributors | White, Olivia Masih |
| Publisher | University of North Texas |
| Source Sets | University of North Texas |
| Language | English |
| Detected Language | English |
| Type | Thesis or Dissertation |
| Format | Text |
| Rights | Public, Robinett, Sheldon J. (Sheldon Jay), Copyright, Copyright is held by the author, unless otherwise noted. All rights reserved. |
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