Prader-Willi Syndrome (PWS) First description Prader-Willi syndrome (PWS) was first described in 1956 by Prader, Labhart and Willi. Genetics and molecular biology PWS results from the absence of expression of the paterna - Small nucleolar RNA SNORD116 - Document - PDFSEARCH.IO

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	Prader-Willi Syndrome (PWS) First description Prader-Willi syndrome (PWS) was first described in 1956 by Prader, Labhart and Willi. Genetics and molecular biology PWS results from the absence of expression of the paterna Add to Reading List Document Date: 2015-05-13 15:34:08 Open Document File Size: 267,62 KB Share Result on Facebook Country Netherlands / / IndustryTerm food intake / http / MedicalCondition autism spectrum disorders / Infertility / hypersomnia / severe psychiatric disorders / Prader-Willi Syndrome / Prader Willi syndrome / Prader- Willi syndrome / severe hypotonia / obesity / psychotic illness / Dementia / hypogonadism / First description Prader-Willi syndrome / psychiatric illness / nonspecific mental retardation / defined psychiatric disorder / difficult-to-treat illness / daytime hypersomnolence / steroidal sex hormone deficiency / dysfunction / Autism / Dementias / Down syndrome / / MedicalTreatment gastric banding / / Person Int J Obes / Sarita Soni / / Position Butler / Clarke D.J. / / Technology genotype / / URL http / SocialTag Syndromes Genodermatoses Prader–Willi syndrome Cytogenetics Small nuclear RNA Genomic imprinting Small nucleolar RNA SNORD116 Chromosome 15 Uniparental disomy Genetics

Prader-Willi Syndrome (PWS) First description Prader-Willi syndrome (PWS) was first described in 1956 by Prader, Labhart and Willi. Genetics and molecular biology PWS results from the absence of expression of the paternaAdd to Reading List