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Stephanie Austin

Showing results (31-40 of 34) with videos related to

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Molecular Genetics and Metabolism|September 14, 2011
Common mutation in the PHKA2 gene with variable phenotype in patients with liver phosphorylase b kinase deficiencySamira Achouitar, Jennifer L Goldstein, Miski Mohamed, et al.
Current Opinion in Hematology|November 20, 2018
Neutropenia in glycogen storage disease Ib: outcomes for patients treated with granulocyte colony-stimulating factorDavid C Dale, Audrey Anna Bolyard, Tracy Marrero, et al.
Orphanet Journal of Rare Diseases|January 27, 2016
Diagnosis of late-onset Pompe disease and other muscle disorders by next-generation sequencingSébastien Lévesque, Christiane Auray-Blais, Elaine Gravel, et al.
Wiley Interdisciplinary Reviews. Climate Change|September 27, 2016
Community-based adaptation research in the Canadian ArcticJames D Ford, Ellie Stephenson, Ashlee Cunsolo Willox, et al.
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Showing results (31-40 of 34) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 34 results.
Molecular Genetics and Metabolism|September 14, 2011
Common mutation in the PHKA2 gene with variable phenotype in patients with liver phosphorylase b kinase deficiencySamira Achouitar, Jennifer L Goldstein, Miski Mohamed, et al.
Current Opinion in Hematology|November 20, 2018
Neutropenia in glycogen storage disease Ib: outcomes for patients treated with granulocyte colony-stimulating factorDavid C Dale, Audrey Anna Bolyard, Tracy Marrero, et al.
Orphanet Journal of Rare Diseases|January 27, 2016
Diagnosis of late-onset Pompe disease and other muscle disorders by next-generation sequencingSébastien Lévesque, Christiane Auray-Blais, Elaine Gravel, et al.
Wiley Interdisciplinary Reviews. Climate Change|September 27, 2016
Community-based adaptation research in the Canadian ArcticJames D Ford, Ellie Stephenson, Ashlee Cunsolo Willox, et al.
Pageof 4