Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
3 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Multi-gene testing in neurological disorders showed an improved diagnostic yield: data from over 1000 Indian patients.
J Neurol. 2019 Aug;266(8):1919-1926. doi: 10.1007/s00415-019-09358-1. Epub 2019 May 8.
J Neurol. 2019.
PMID: 31069529
Detection of high frequency of mutations in a breast and/or ovarian cancer cohort: implications of embracing a multi-gene panel in molecular diagnosis in India.
Mannan AU, Singh J, Lakshmikeshava R, Thota N, Singh S, Sowmya TS, Mishra A, Sinha A, Deshwal S, Soni MR, Chandrasekar A, Ramesh B, Ramamurthy B, Padhi S, Manek P, Ramalingam R, Kapoor S, Ghosh M, Sankaran S, Ghosh A, Veeramachaneni V, Ramamoorthy P, Hariharan R, Subramanian K.
Mannan AU, et al. Among authors: soni mr.
J Hum Genet. 2016 Jun;61(6):515-22. doi: 10.1038/jhg.2016.4. Epub 2016 Feb 25.
J Hum Genet. 2016.
PMID: 26911350
Item in Clipboard
Tetralogy of Fallot with restrictive ventricular septal defect by accessory tricuspid leaflet tissue.
Soni MR, Bohara DA, Mahajan AU, Nathani PJ.
Soni MR, et al.
Indian Heart J. 2012 Jul-Aug;64(4):412-5. doi: 10.1016/j.ihj.2012.06.009. Epub 2012 Jun 22.
Indian Heart J. 2012.
PMID: 22929828
Free PMC article.
Item in Clipboard
Cite
Cite