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 withi...
| Main Author: | |
|---|---|
| Format: | Others |
| Language: | English |
| Published: |
University of North Texas
1994
|
| Subjects: | |
| Online Access: | https://digital.library.unt.edu/ark:/67531/metadc332745/ |