Familial whole Exome Sequencing to Identify Genetic Variants Associated with Polycystic Ovarian Syndrome in Indians

dc.contributor.guide	Usha.B
dc.coverage.spatial
dc.creator.researcher	Dakshina Moorthy Janani
dc.date.accessioned	2021-09-15T04:35:51Z
dc.date.available	2021-09-15T04:35:51Z
dc.date.awarded
dc.date.completed	2021
dc.date.registered
dc.description.abstract	Polycystic Ovary Syndrome (PCOS) is an endocrinological gynecology disorder with heterogeneous representation of the clinical symptoms among its patients. Due to this dynamic nature there is a lack of consensus in the medical community for the diagnosis and treatment. The pathophysiology not being clearly understood adds on to the discrepancies. Genetics has been reported to be a major etiology of PCOS, which is a complex disorder following a non-mendelian pattern of inheritance newline
dc.description.note
dc.format.accompanyingmaterial	DVD
dc.format.dimensions
dc.format.extent
dc.identifier.uri	http://hdl.handle.net/10603/340536
dc.language	English
dc.publisher.institution	Department of Biotechnology
dc.publisher.place	Kattankulathur
dc.publisher.university	SRM University
dc.relation
dc.rights	university
dc.source.university	University
dc.subject.keyword	Ecology
dc.subject.keyword	Ecology and Environment
dc.subject.keyword	Life Sciences
dc.title	Familial whole Exome Sequencing to Identify Genetic Variants Associated with Polycystic Ovarian Syndrome in Indians
dc.title.alternative
dc.type.degree	Ph.D.