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Imprinting and Genetic Disease: Angelman, Prader-Willi and Beckwith-Weidemann Syndromes | Learn Science at Scitable
![Karyotype of Prader-Willi syndrome, computer illustration. This is a genetic disorder caused by the deletion of a region on chromosome 15 inherited fr Stock Photo - Alamy Karyotype of Prader-Willi syndrome, computer illustration. This is a genetic disorder caused by the deletion of a region on chromosome 15 inherited fr Stock Photo - Alamy](https://c8.alamy.com/comp/2CP4EA6/karyotype-of-prader-willi-syndrome-computer-illustration-this-is-a-genetic-disorder-caused-by-the-deletion-of-a-region-on-chromosome-15-inherited-fr-2CP4EA6.jpg)
Karyotype of Prader-Willi syndrome, computer illustration. This is a genetic disorder caused by the deletion of a region on chromosome 15 inherited fr Stock Photo - Alamy
![Genetics of Childhood Disorders: XII. Genomic Imprinting: Breaking the Rules - Journal of the American Academy of Child & Adolescent Psychiatry Genetics of Childhood Disorders: XII. Genomic Imprinting: Breaking the Rules - Journal of the American Academy of Child & Adolescent Psychiatry](https://www.jaacap.org/cms/attachment/2b79d965-2e41-43ff-99ac-4fb45039fefc/gr1.jpg)
Genetics of Childhood Disorders: XII. Genomic Imprinting: Breaking the Rules - Journal of the American Academy of Child & Adolescent Psychiatry
Ontario Prader-Willi Syndrome Association - Prader-Willi Syndrome (PWS) is a rare genetic disorder that is an abnormality on the 15th chromosome. In most cases, the genetic error that causes PWS occurs at
![Karyotype of prader-willi syndrome, labelled 3d illustration. a genetic disorder caused by a lack of function of part of | CanStock Karyotype of prader-willi syndrome, labelled 3d illustration. a genetic disorder caused by a lack of function of part of | CanStock](https://cdn.w600.comps.canstockphoto.com/karyotype-of-prader-willi-syndrome-stock-photo_csp84381445.jpg)
Karyotype of prader-willi syndrome, labelled 3d illustration. a genetic disorder caused by a lack of function of part of | CanStock
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Familial inheritance of imprinting centre (IC) deletions in Angelman... | Download Scientific Diagram
![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
![Baby food and bedtime: Evidence for opposite phenotypes from different genetic and epigenetic alterations in Prader-Willi and Angelman syndromes - Iiro Ilmari Salminen, Bernard J Crespi, Mikael Mokkonen, 2019 Baby food and bedtime: Evidence for opposite phenotypes from different genetic and epigenetic alterations in Prader-Willi and Angelman syndromes - Iiro Ilmari Salminen, Bernard J Crespi, Mikael Mokkonen, 2019](https://journals.sagepub.com/cms/10.1177/2050312118823585/asset/images/large/10.1177_2050312118823585-fig2.jpeg)