Chromosome 22q11 deletion in patients with selected congenital heart disease conotruncal malformations: study of prevalence phenotype genotype and mode of inheritance

dc.contributor.guide	Kumar, R Krishna and Vasudevan, D M	en_US
dc.coverage.spatial	Allied Health Sciences	en_US
dc.creator.researcher	Alka Anilkumar	en_US
dc.date.accessioned	2015-05-09T10:57:32Z
dc.date.available	2015-05-09T10:57:32Z
dc.date.awarded	n.d.	en_US
dc.date.completed	2013	en_US
dc.date.issued	2015-05-09
dc.date.registered	n.d.	en_US
dc.description.abstract	Abstract Available	en_US
dc.description.note	References p.147-189	en_US
dc.format.accompanyingmaterial	None	en_US
dc.format.dimensions	-	en_US
dc.format.extent	189p.	en_US
dc.identifier.uri	http://hdl.handle.net/10603/40982
dc.language	English	en_US
dc.publisher.institution	Department of Public Health Dentistry	en_US
dc.publisher.place	Coimbatore	en_US
dc.publisher.university	Amrita Vishwa Vidyapeetham (University)	en_US
dc.relation	-	en_US
dc.rights	university	en_US
dc.source.inflibnet	INFLIBNET	en_US
dc.subject.keyword	Chromosome	en_US
dc.subject.keyword	congenital heart	en_US
dc.subject.keyword	heart disease	en_US
dc.subject.keyword	patients	en_US
dc.title	Chromosome 22q11 deletion in patients with selected congenital heart disease conotruncal malformations: study of prevalence phenotype genotype and mode of inheritance	en_US
dc.title.alternative	study of prevalence phenotype genotype and mode of inheritance	en_US
dc.type.degree	Ph.D.	en_US