1. Shodhganga@INFLIBNET
  2. University of Delhi
  3. Dept. of Genetics
Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/489347
Title: Identification of rare putative causal gene variants in Intellectual disability and Parkinson s disease families
Researcher: Laxmi
Guide(s): Thelma, B.K.
Keywords: disability and Parkinson
Genetics and Heredity
Life Sciences
Molecular Biology and Genetics
University: University of Delhi
Completed Date: 2017
Abstract: Available
Pagination: 196 p.
URI: http://hdl.handle.net/10603/489347
Appears in Departments:Dept. of Genetics

Files in This Item:
File Description SizeFormat 
01_title.pdfAttached File157.03 kBAdobe PDFView/Open
02_prelim pages.pdf472.71 kBAdobe PDFView/Open
03_table of content.pdf176.52 kBAdobe PDFView/Open
04_abstract.pdf237.29 kBAdobe PDFView/Open
05_chapter 1.pdf2.02 MBAdobe PDFView/Open
06_chapter 2.pdf1.02 MBAdobe PDFView/Open
07_chapter 3.pdf808.79 kBAdobe PDFView/Open
08_chapter 4.pdf1.22 MBAdobe PDFView/Open
09_chapter 5.pdf573.65 kBAdobe PDFView/Open
10_annexture.pdf691.49 kBAdobe PDFView/Open
80_recommendation.pdf276.22 kBAdobe PDFView/Open
Show full item record


Items in Shodhganga are licensed under Creative Commons Licence Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0).

Altmetric Badge: