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K D Jain

Showing results (1-10 of 7) with videos related to

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The Indian Medical Gazette|October 11, 2017
A Case of Rheumatic ChoreaK D Jain
The Indian Medical Gazette|October 11, 2017
A Case of PolymastiaK D Jain
Pediatric Neurology|January 1, 1996
MERRF syndrome with overwhelming lactic acidosisT D Sanger, K D Jain
American Journal of Human Genetics|July 1, 1996
A rational approach to cystic fibrosis mutation analysis in Hispanics: reply to Arzimanoglou et alT A Grebe, W W Doane, S F Richter, et al.
Annals of the Royal College of Surgeons of England|October 30, 2016
Nine-year results of whole femoral head allograft with articular cartilage for acetabular impaction grafting in revision hip replacementE Drampalos, A Fadulelmola, R Mohammed, et al.
Neurology|May 1, 1994
A T-->C mutation at nt 8993 of mitochondrial DNA in a child with Leigh syndromeF M Santorelli, S Shanske, K D Jain, et al.
Pediatric Research|May 1, 1996
Clinical heterogeneity associated with the mitochondrial DNA T8993C point mutationF M Santorelli, S C Mak, M E Vazquez-Memije, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
The Indian Medical Gazette|October 11, 2017
A Case of Rheumatic ChoreaK D Jain
The Indian Medical Gazette|October 11, 2017
A Case of PolymastiaK D Jain
Pediatric Neurology|January 1, 1996
MERRF syndrome with overwhelming lactic acidosisT D Sanger, K D Jain
American Journal of Human Genetics|July 1, 1996
A rational approach to cystic fibrosis mutation analysis in Hispanics: reply to Arzimanoglou et alT A Grebe, W W Doane, S F Richter, et al.
Annals of the Royal College of Surgeons of England|October 30, 2016
Nine-year results of whole femoral head allograft with articular cartilage for acetabular impaction grafting in revision hip replacementE Drampalos, A Fadulelmola, R Mohammed, et al.
Neurology|May 1, 1994
A T-->C mutation at nt 8993 of mitochondrial DNA in a child with Leigh syndromeF M Santorelli, S Shanske, K D Jain, et al.
Pediatric Research|May 1, 1996
Clinical heterogeneity associated with the mitochondrial DNA T8993C point mutationF M Santorelli, S C Mak, M E Vazquez-Memije, et al.
Pageof 1