![Prader–Willi Syndrome and Angelman Syndrome in Cousins from a Family with a Translocation between Chromosomes 6 and 15 | NEJM Prader–Willi Syndrome and Angelman Syndrome in Cousins from a Family with a Translocation between Chromosomes 6 and 15 | NEJM](https://www.nejm.org/na101/home/literatum/publisher/mms/journals/content/nejm/1992/nejm_1992.326.issue-12/nejm199203193261206/production/images/img_medium/nejm199203193261206_f3.jpeg)
Prader–Willi Syndrome and Angelman Syndrome in Cousins from a Family with a Translocation between Chromosomes 6 and 15 | NEJM
Clinical Trial for Cannabidiol Effect on Hyperphagia in Affected Individuals with Prader-Willi Syndrome | Cannabis Sciences
The Foundation for Prader-Willi Research - PWS is caused by a lack of active genetic material in a particular region of chromosome 15 (15q11-q13). Normally, individuals inherit one copy of chromosome 15
![Prader–Willi Syndrome and Angelman Syndrome in Cousins from a Family with a Translocation between Chromosomes 6 and 15 | NEJM Prader–Willi Syndrome and Angelman Syndrome in Cousins from a Family with a Translocation between Chromosomes 6 and 15 | NEJM](https://www.nejm.org/na101/home/literatum/publisher/mms/journals/content/nejm/1992/nejm_1992.326.issue-12/nejm199203193261206/production/images/img_medium/nejm199203193261206_f5.jpeg)
Prader–Willi Syndrome and Angelman Syndrome in Cousins from a Family with a Translocation between Chromosomes 6 and 15 | NEJM
![PDF] Genetic changes of chromosome region 15q11-q13 in Prader-Willi and Angelman syndromes in Finland | Semantic Scholar PDF] Genetic changes of chromosome region 15q11-q13 in Prader-Willi and Angelman syndromes in Finland | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/b4ea7a242439c2c0cca3b709475036f36012c941/20-Figure1-1.png)
PDF] Genetic changes of chromosome region 15q11-q13 in Prader-Willi and Angelman syndromes in Finland | Semantic Scholar
![Prenatal diagnosis of Prader–Willi syndrome and Angelman syndrome for fetuses with suspicious deletion of chromosomal region 15q11-q13 - ScienceDirect Prenatal diagnosis of Prader–Willi syndrome and Angelman syndrome for fetuses with suspicious deletion of chromosomal region 15q11-q13 - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0020729213006723-gr1.jpg)