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L Leclerc

Showing results (151-160 of 155) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|February 19, 1998
Risk and penetrance of primary hyperparathyroidism in multiple endocrine neoplasia type 2A families with mutations at codon 634 of the RET proto-oncogene. Groupe D'etude des Tumeurs à CalcitonineI Schuffenecker, M Virally-Monod, R Brohet, et al.
Equine Veterinary Journal. Supplement|November 10, 2010
Effect of a 120 km endurance race on plasma and muscular neutrophil elastase and myeloperoxidase concentrations in horsesD Serteyn, C Sandersen, J-P Lejeune, et al.
Neurology|March 7, 2008
New VAPB deletion variant and exclusion of VAPB mutations in familial ALSJ E Landers, A L Leclerc, L Shi, et al.
Neurology|April 7, 2019
Haptoglobin genotype and aneurysmal subarachnoid hemorrhage: Individual patient data analysisBen Gaastra, Dianxu Ren, Sheila Alexander, et al.
Science (New York, N.Y.)|March 3, 2009
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosisT J Kwiatkowski, D A Bosco, A L Leclerc, et al.
Pageof 16

Showing results (151-160 of 155) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 155 results.
The Journal of Clinical Endocrinology and Metabolism|February 19, 1998
Risk and penetrance of primary hyperparathyroidism in multiple endocrine neoplasia type 2A families with mutations at codon 634 of the RET proto-oncogene. Groupe D'etude des Tumeurs à CalcitonineI Schuffenecker, M Virally-Monod, R Brohet, et al.
Equine Veterinary Journal. Supplement|November 10, 2010
Effect of a 120 km endurance race on plasma and muscular neutrophil elastase and myeloperoxidase concentrations in horsesD Serteyn, C Sandersen, J-P Lejeune, et al.
Neurology|March 7, 2008
New VAPB deletion variant and exclusion of VAPB mutations in familial ALSJ E Landers, A L Leclerc, L Shi, et al.
Neurology|April 7, 2019
Haptoglobin genotype and aneurysmal subarachnoid hemorrhage: Individual patient data analysisBen Gaastra, Dianxu Ren, Sheila Alexander, et al.
Science (New York, N.Y.)|March 3, 2009
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosisT J Kwiatkowski, D A Bosco, A L Leclerc, et al.
Pageof 16