Genome wide detection of human copy number variations in dyslexic families from south India using microarray based SNP and CNV array six point zero

dc.contributor.guide	Ramachandra, N. B.	en_US
dc.coverage.spatial		en_US
dc.creator.researcher	Avinash M. V.	en_US
dc.date.accessioned	2015-03-13T04:35:08Z
dc.date.available	2015-03-13T04:35:08Z
dc.date.awarded		en_US
dc.date.completed	2013	en_US
dc.date.issued	2015-03-13
dc.date.registered		en_US
dc.description.abstract	newline	en_US
dc.description.note		en_US
dc.format.accompanyingmaterial	None	en_US
dc.format.dimensions		en_US
dc.format.extent		en_US
dc.identifier.uri	http://hdl.handle.net/10603/37083
dc.language	English	en_US
dc.publisher.institution	Department of Studies in Zoology	en_US
dc.publisher.place	Mysore	en_US
dc.publisher.university	University of Mysore	en_US
dc.relation		en_US
dc.rights	university	en_US
dc.source.university	University	en_US
dc.subject.keyword	Genetics	en_US
dc.subject.keyword	Genetic Variation	en_US
dc.subject.keyword	Human cytogenetics	en_US
dc.subject.keyword	Human genetics	en_US
dc.subject.keyword	Human genome	en_US
dc.subject.keyword	SNP and CNV Array	en_US
dc.title	Genome wide detection of human copy number variations in dyslexic families from south India using microarray based SNP and CNV array six point zero	en_US
dc.title.alternative		en_US
dc.type.degree	Ph.D.	en_US