SOCIETY FOR THE STUDY OF BEHAVIOURAL PHENOTYPES An International Organisation The SSBP is a Registered Charity: Charity No:Prader-Willi Syndrome (PWS)

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Date: 2013-02-13 00:06:40 Syndromes Genodermatoses Prader–Willi syndrome Cytogenetics Small nuclear RNA Genomic imprinting Small nucleolar RNA SNORD116 Chromosome 15 Uniparental disomy Genetics Health Biology		SOCIETY FOR THE STUDY OF BEHAVIOURAL PHENOTYPES An International Organisation The SSBP is a Registered Charity: Charity No:Prader-Willi Syndrome (PWS) Add to Reading List Source URL: www.qcidd.com.au Download Document from Source Website File Size: 31,51 KB Share Document on Facebook

	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 DocID: 19j07 - View Document
	Common nomenclature of ID names and major common molecular findings Chromosome Suggested Name DocID: 14ZUT - View Document
	SOCIETY FOR THE STUDY OF BEHAVIOURAL PHENOTYPES An International Organisation The SSBP is a Registered Charity: Charity No:Prader-Willi Syndrome (PWS) DocID: 14Mho - View Document
	BRIEF REPORT An ABCC8 Gene Mutation and Mosaic Uniparental Isodisomy Resulting in Atypical Diffuse Congenital Hyperinsulinism Khalid Hussain,1 Sarah E. Flanagan,2 Virpi V. Smith,3 Michael Ashworth,3 Michael Day,4 DocID: RWUD - View Document
	HUMAN MUTATION 22:92^[removed]METHODS Epigenetic Detection of Human Chromosome 14 Uniparental Disomy DocID: NLhC - View Document