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Chromosome 15
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#	Item
21	What is Angelman Syndrome? Angelman Syndrome (AS) is a rare neuro-genetic disorder named after an English paediatrician, Dr Harry Angelman, who first described the syndrome inThe AS gene Add to Reading List Source URL: www.qcidd.com.au Language: English - Date: 2013-07-26 01:42:28 Syndromes Genodermatoses Neurological disorders Angelman syndrome Cytogenetics Harry Angelman Chromosome 15 UBE3A Genomic imprinting Genetics Health Biology
22	Charity No Legal and Administrative Details For the Year Ended 31 March 2006 Status Add to Reading List Source URL: www.rarechromo.org Language: English - Date: 2006-07-13 14:20:12 Cytogenetics Syndromes Chromosome Human genome Human genetics Karyotype XYY syndrome Isodicentric 15 1q21.1 duplication syndrome Biology Genetics Philosophy of biology
23	Angelman Syndrome Background This neurodevelopmental disorder, once termed “happy puppet” due to the happy disposition and characteristic movement disorder of the patients, was first described in 1965 by Harry Angelm Add to Reading List Source URL: www.cddh.monash.org Language: English - Date: 2012-03-27 18:24:05 Syndromes Genodermatoses Rare diseases Pervasive developmental disorders Angelman syndrome Chromosome 15 Rett syndrome Developmental disorder Epilepsy Health Medicine Neurological disorders
24	Please help us support mo re children born sick and disabled ers by rare chromosome disord Add to Reading List Source URL: www.rarechromo.org Language: English - Date: 2014-05-23 09:08:54 Syndromes Chromosome Medical genetics Isodicentric 15 X chromosome Genetics Biology Cytogenetics
25	Angelman Syndrome Information Sheet - to be included in the Personal Health Record of people who have been diagnosed as having Angelman Syndrome The material in this sheet has been adapted from the Therapeutic Guideline Add to Reading List Source URL: www.cddh.monash.org Language: English - Date: 2012-03-27 00:19:02 Syndromes Angelman syndrome Rett syndrome Chromosome 15 Epilepsy Developmental disorder Autism Neurodevelopmental disorder Mental disorder Health Neurological disorders Medicine
26	clinical Prader-Willi syndrome Care of adults in general practice Elly Scheermeyer Add to Reading List Source URL: www.racgp.org.au Language: English - Date: 2013-01-20 17:11:19 Syndromes Genodermatoses Growth hormones Prader–Willi syndrome Growth hormone treatment Obesity Chromosome 15 Growth hormone deficiency Hypotonia Health Medicine Biology
27	The Unique Garden at Hampton Court Palace Flower Show 2015 Sponsor A Plant Appeal We would like to thank the following people for their extremely kind donations, to sponsor a plant for the Unique Garden at the Hampton Co Add to Reading List Source URL: www.rarechromo.org Language: English - Date: 2015-04-14 09:48:34 Biology Cytogenetics Chromosome Isodicentric 15 X chromosome DiGeorge syndrome 22q13 deletion syndrome 1q21.1 deletion syndrome 1q21.1 duplication syndrome Genetics Health Syndromes
28	Rare Chromosome Disorder Support Group Reference and Administrative Details For The Year Ended 31 March 2007 Company Number Add to Reading List Source URL: www.rarechromo.org Language: English - Date: 2007-09-23 16:09:11 Chromosome Cytogenetics Syndromes Human genome Rare disease Isodicentric 15 Genetics Biology Philosophy of biology
29	Dear Educator, This file offers views of some of the worksheets in our “Heredity” thematic unit. The cover for an eWorkbook is shown followed by the preview pages. The “Heredity” unit offers 15 pages. Add to Reading List Source URL: www.ishoptoday.com Language: English - Date: 2014-07-28 11:06:52 Chromosome Gene Phenotypic trait Biology Genetics Heredity
30	OPEN Citation: Cell Death and Disease[removed], e1625; doi:[removed]cddis[removed] & 2015 Macmillan Publishers Limited All rights reserved[removed]www.nature.com/cddis Add to Reading List Source URL: www.nature.com Language: English - Date: 2015-01-29 08:34:01 Apoptosis Genes UBE3A Chromosome 15 Ubiquitin HECT domain Proteasome Mdm2 P53 Biology Proteins Posttranslational modification