## Abstract PraderβWilli syndrome (PWS) is caused by the disturbed expression of genes from the imprinted region of 15q11βq13, but the specific contributions of individual genes remain unknown. Most paternal PWS deletions are bracketed by recurrent breakpoints BP1 or BP2 and BP3. Atypical deletions
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The Prader-Willi syndrome and interstitial deletion of chromosome 15: High-resolution chromosome analyses of 14 patients with the Prader-Willi syndrome and of 5 suspected infants
β Scribed by Yoshimitsu Fukushima; Norio Niikawa; Yoshikazu Kuroki
- Publisher
- Nature Publishing Group
- Year
- 1984
- Tongue
- English
- Weight
- 392 KB
- Volume
- 29
- Category
- Article
- ISSN
- 1435-232X
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