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J T R Clarke

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

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Lancet (London, England)|December 5, 2009
Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry dataA Mehta, M Beck, P Elliott, et al.
Fetal Diagnosis and Therapy|March 27, 2009
Intracerebral periventricular pseudocysts in a fetus with mitochondrial depletion syndrome: an association or coincidenceM Rohrbach, D Chitayat, G Maegawa, et al.
Neuroradiology|August 13, 2016
Validation of the finding of hypertrophy of the clava in infantile neuroaxonal dystrophy/PLA2G6 by biometric analysisA Al-Maawali, G Yoon, A S Feigenbaum, et al.
Molecular Genetics and Metabolism|August 29, 2007
Development of a clinical assay for detection of GAA mutations and characterization of the GAA mutation spectrum in a Canadian cohort of individuals with glycogen storage disease, type IIM E McCready, N L Carson, P Chakraborty, et al.
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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.
Lancet (London, England)|December 5, 2009
Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry dataA Mehta, M Beck, P Elliott, et al.
Fetal Diagnosis and Therapy|March 27, 2009
Intracerebral periventricular pseudocysts in a fetus with mitochondrial depletion syndrome: an association or coincidenceM Rohrbach, D Chitayat, G Maegawa, et al.
Neuroradiology|August 13, 2016
Validation of the finding of hypertrophy of the clava in infantile neuroaxonal dystrophy/PLA2G6 by biometric analysisA Al-Maawali, G Yoon, A S Feigenbaum, et al.
Molecular Genetics and Metabolism|August 29, 2007
Development of a clinical assay for detection of GAA mutations and characterization of the GAA mutation spectrum in a Canadian cohort of individuals with glycogen storage disease, type IIM E McCready, N L Carson, P Chakraborty, et al.
Pageof 2