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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Rare Diseases
Last data update: Apr 21, 2024
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Prader-willi Syndrome[original query]>>Reviews/Commentaries[Product Type]
Biological, Behavioral, and Ethical Considerations of Prader-Willi Syndrome: A Primer for Behavior Analysts.
Kennedy Danielle et al. Behavior analysis in practice 2022 15(2) 562-570
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A scoping review of case law relating to support and treatment for people with Prader-Willi Syndrome.
Murray Anna et al. International journal of law and psychiatry 2021 78101733
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Clinical epigenetics: a primer for the practitioner.
Aygun Deniz et al. Developmental medicine and child neurology 2019 Nov
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Prader-Willi Syndrome - Clinical Genetics, Diagnosis and Treatment Approaches: An Update.
Butler Merlin G et al. Current pediatric reviews 2019 Jul
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When a Rare Mutation Causes a Rare Disease: Jacob�s Story
R Lewis, PLOS Blogs, June 20, 2019
PRADER-WILLI SYNDROME: WHAT IS THE GENERAL PEDIATRICIAN SUPPOSED TO DO? - A REVIEW.
Passone Caroline Buff Gouveia et al. Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo 36(3) 345-352
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A Review of the Genomic Analysis of Children Presenting with Developmental Delay/Intellectual Disability and Associated Dysmorphic Features.
Vickers Ramiah R et al. Cureus 2019 Jan 11(1) e3873
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A multidisciplinary approach to the clinical management of Prader-Willi syndrome.
Duis Jessica et al. Molecular genetics & genomic medicine 2019 Jan
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Benefits and Limitations of Prenatal Screening for Prader-Willi Syndrome.
Butler Merlin G et al. Prenatal diagnosis 2016 Aug
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 21, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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