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S G Mehta

Showing results (11-20 of 14) with videos related to

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Clinical Genetics|October 16, 2007
Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementiaG D J Watts, D Thomasova, S K Ramdeen, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|May 31, 2017
Lessons Learned: Early Termination of a Randomized Trial of Calcineurin Inhibitor and Corticosteroid Avoidance Using BelataceptK A Newell, A K Mehta, C P Larsen, et al.
Prenatal Diagnosis|June 19, 2026
Is There Potential Clinical Utility in Reporting Variants of Uncertain Significance From Prenatal Sequencing?A Gibbs, R Braham, V Ramachandran, et al.
Clinical Genetics|August 23, 2012
Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementiaS G Mehta, M Khare, R Ramani, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Clinical Genetics|October 16, 2007
Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementiaG D J Watts, D Thomasova, S K Ramdeen, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|May 31, 2017
Lessons Learned: Early Termination of a Randomized Trial of Calcineurin Inhibitor and Corticosteroid Avoidance Using BelataceptK A Newell, A K Mehta, C P Larsen, et al.
Prenatal Diagnosis|June 19, 2026
Is There Potential Clinical Utility in Reporting Variants of Uncertain Significance From Prenatal Sequencing?A Gibbs, R Braham, V Ramachandran, et al.
Clinical Genetics|August 23, 2012
Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementiaS G Mehta, M Khare, R Ramani, et al.
Pageof 2