![SciELO - Brasil - Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes SciELO - Brasil - Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes](https://minio.scielo.br/documentstore/1678-4685/GPTn6WZcKspMbDnLRHZ6RCd/f00e84ecef77b96975e48ac07c92a2b0a087870c.jpg)
SciELO - Brasil - Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes Genomic imprinting: genetic mechanisms and phenotypic consequences in Prader-Willi and Angelman syndromes
![Diseases | Free Full-Text | Prader-Willi Syndrome: The Disease that Opened up Epigenomic-Based Preemptive Medicine | HTML Diseases | Free Full-Text | Prader-Willi Syndrome: The Disease that Opened up Epigenomic-Based Preemptive Medicine | HTML](https://www.mdpi.com/diseases/diseases-04-00015/article_deploy/html/images/diseases-04-00015-g002.png)
Diseases | Free Full-Text | Prader-Willi Syndrome: The Disease that Opened up Epigenomic-Based Preemptive Medicine | HTML
![Frontiers | The Autism and Angelman Syndrome Protein Ube3A/E6AP: The Gene, E3 Ligase Ubiquitination Targets and Neurobiological Functions | Molecular Neuroscience Frontiers | The Autism and Angelman Syndrome Protein Ube3A/E6AP: The Gene, E3 Ligase Ubiquitination Targets and Neurobiological Functions | Molecular Neuroscience](https://www.frontiersin.org/files/Articles/448792/fnmol-12-00109-HTML/image_m/fnmol-12-00109-g001.jpg)
Frontiers | The Autism and Angelman Syndrome Protein Ube3A/E6AP: The Gene, E3 Ligase Ubiquitination Targets and Neurobiological Functions | Molecular Neuroscience
![PDF) Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis | Dvorah Abeliovich and K. Buiting - Academia.edu PDF) Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis | Dvorah Abeliovich and K. Buiting - Academia.edu](https://0.academia-photos.com/attachment_thumbnails/45367870/mini_magick20190212-11658-14uz0bj.png?1549983975)
PDF) Sporadic Imprinting Defects in Prader-Willi Syndrome and Angelman Syndrome: Implications for Imprint-Switch Models, Genetic Counseling, and Prenatal Diagnosis | Dvorah Abeliovich and K. Buiting - Academia.edu
Full article: Prader-Willi syndrome and Angelman syndrome: Visualisation of the molecular pathways for two chromosomal disorders
![PWS-AS Region Schematic representation of the Prader-Willi syndrome and... | Download Scientific Diagram PWS-AS Region Schematic representation of the Prader-Willi syndrome and... | Download Scientific Diagram](https://www.researchgate.net/profile/Valter-Tucci/publication/332320528/figure/fig3/AS:818227538042882@1572092055813/PWS-AS-Region-Schematic-representation-of-the-Prader-Willi-syndrome-and-Angelman-syndrome_Q640.jpg)
PWS-AS Region Schematic representation of the Prader-Willi syndrome and... | Download Scientific Diagram
![Clinical, molecular genetics and therapeutic aspects of syndromic obesity - Geets - 2019 - Clinical Genetics - Wiley Online Library Clinical, molecular genetics and therapeutic aspects of syndromic obesity - Geets - 2019 - Clinical Genetics - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/fffe4fae-d0aa-486d-9b9a-7ed5c23391c0/cge13367-fig-0002-m.jpg)
Clinical, molecular genetics and therapeutic aspects of syndromic obesity - Geets - 2019 - Clinical Genetics - Wiley Online Library
![Prevalence of Angelman syndrome and Prader–Willi syndrome in Estonian children: Sister syndromes not equally represented - Õiglane‐Shlik - 2006 - American Journal of Medical Genetics Part A - Wiley Online Library Prevalence of Angelman syndrome and Prader–Willi syndrome in Estonian children: Sister syndromes not equally represented - Õiglane‐Shlik - 2006 - American Journal of Medical Genetics Part A - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/5b1a197b-f2a5-4722-b1c8-2f398dc69cdc/mfig002.jpg)
Prevalence of Angelman syndrome and Prader–Willi syndrome in Estonian children: Sister syndromes not equally represented - Õiglane‐Shlik - 2006 - American Journal of Medical Genetics Part A - Wiley Online Library
![Genes | Free Full-Text | The Global Prader–Willi Syndrome Registry: Development, Launch, and Early Demographics | HTML Genes | Free Full-Text | The Global Prader–Willi Syndrome Registry: Development, Launch, and Early Demographics | HTML](https://www.mdpi.com/genes/genes-10-00713/article_deploy/html/images/genes-10-00713-g001.png)
Genes | Free Full-Text | The Global Prader–Willi Syndrome Registry: Development, Launch, and Early Demographics | HTML
![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_t1.jpeg)
Prader–Willi Syndrome and Angelman Syndrome in Cousins from a Family with a Translocation between Chromosomes 6 and 15 | NEJM
![PDF) Prevalence of Angelman syndrome and Prader–Willi syndrome in Estonian children: Sister syndromes not equally represented | Gunnar Tasa - Academia.edu PDF) Prevalence of Angelman syndrome and Prader–Willi syndrome in Estonian children: Sister syndromes not equally represented | Gunnar Tasa - Academia.edu](https://0.academia-photos.com/attachment_thumbnails/40858967/mini_magick20190220-8762-1ks9q0t.png?1550677536)