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Chromosome 15
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#	Item
11	Angelman Syndrome Alternative names Although the term ‘happy puppet syndrome’, proposed by Bower and Jeavons in 1967 was widely used until the early 1990’s, the eponym ‘Angelman’ syndrome is generally preferred Add to Reading List Source URL: www.ssbp.org.uk Language: English - Date: 2015-05-13 15:34:24 Syndromes Genodermatoses Neurological disorders Genes Cytogenetics Angelman syndrome UBE3A Chromosome 15 Prader–Willi syndrome Genetics Health Biology
12	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: 2015-05-15 10:47:17 Syndromes Cytogenetics Chromosome Isodicentric 15 X chromosome DiGeorge syndrome 22q13 deletion syndrome 1q21.1 deletion syndrome 1q21.1 duplication syndrome Genetics Health Biology
13	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 Source URL: www.ssbp.org.uk Language: English - Date: 2015-05-13 15:34:08 Syndromes Genodermatoses Prader–Willi syndrome Cytogenetics Small nuclear RNA Genomic imprinting Small nucleolar RNA SNORD116 Chromosome 15 Uniparental disomy Genetics Health Biology
14	T. Whit Athey and James F. Wilson Y-chromosome Haplogroup G includes about 2% of all European men, about 10-15% of Middle Eastern men, and 30-70% in the Caucasus region. Its largest subgroup is Haplogroup G2a3, defined Add to Reading List Source URL: www.jogg.info Language: English - Date: 2008-11-26 07:10:16 Population genetics Haplogroup G Biology Human Y-chromosome DNA haplogroup Haplogroup Genetic genealogy Haplogroup G2a3b1 Haplogroup G2a3a Human evolution Genetics DNA
15	Supplementary figure 1 Schematic representation of DLL4 locus in Homo sapiens chromosome 15, GRCh38 Primary Assembly. DLL4 mRNA starting fromis shown in red boxes; DLL4-AS starting fromand ending at 4 Add to Reading List Source URL: vascularcell.com Language: English DLL4 RNA Homo sapiens
16	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: 2006-07-11 17:44:37 Cytogenetics Syndromes Chromosome Human genome Human genetics Karyotype XYY syndrome Isodicentric 15 1q21.1 duplication syndrome Biology Genetics Philosophy of biology
17	Company noCharity noRare Chromosome Disorder Support Group Report and Audited Financial Statements Add to Reading List Source URL: www.rarechromo.org Language: English - Date: 2011-11-15 10:32:39 Chromosome X chromosome Genetic disorder Karyotype Isodicentric 15 The Focus Foundation Genetics Biology Cytogenetics
18	Unique Accounts 2013.xlsx Add to Reading List Source URL: www.rarechromo.org Language: English - Date: 2013-08-02 06:30:03 Chromosome Human genome Isodicentric 15 Genetics Biology Cytogenetics
19	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 Language: English - 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
20	Angelman Syndrome: an Information Guide for Day Services. Karyn Willoughby BSocSc MSc (Development Studies) For Oakleigh Centre Add to Reading List Source URL: www.cddh.monash.org Language: English - Date: 2014-05-12 02:27:17 Neurological disorders Cytogenetics Syndromes Genodermatoses Angelman syndrome Chromosome 15 UBE3A Harry Angelman Aneuploidy Genetics Health Biology