Debra O Prosser - JoVE Visualize

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Journal of Clinical Medicine Research|July 21, 2017

Splice Site Variants in the KCNQ1 and SCN5A Genes: Transcript Analysis as a Tool in Supporting PathogenicityIvone U S Leong, Philippa A Dryland, Debra O Prosser, et al.

Heart Rhythm|April 2, 2020

Genetic testing in Polynesian long QT syndrome probands reveals a lower diagnostic yield and an increased prevalence of rare variantsAnnika Winbo, Nikki Earle, Luciana Marcondes, et al.

Journal of Inherited Metabolic Disease|October 27, 2015

Brain dopamine-serotonin vesicular transport disease presenting as a severe infantile hypotonic parkinsonian disorderJessie C Jacobsen, Callum Wilson, Vicki Cunningham, et al.

Microarrays (Basel, Switzerland)|September 8, 2016

SNP Analysis and Whole Exome Sequencing: Their Application in the Analysis of a Consanguineous Pedigree Segregating AtaxiaSarah L Nickerson, Renate Marquis-Nicholson, Karen Claxton, et al.

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

Sort By:

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You have reached the last page of results.This site can display upto 14 results.

Journal of Clinical Medicine Research|July 21, 2017

Splice Site Variants in the KCNQ1 and SCN5A Genes: Transcript Analysis as a Tool in Supporting PathogenicityIvone U S Leong, Philippa A Dryland, Debra O Prosser, et al.

Heart Rhythm|April 2, 2020

Genetic testing in Polynesian long QT syndrome probands reveals a lower diagnostic yield and an increased prevalence of rare variantsAnnika Winbo, Nikki Earle, Luciana Marcondes, et al.

Journal of Inherited Metabolic Disease|October 27, 2015

Brain dopamine-serotonin vesicular transport disease presenting as a severe infantile hypotonic parkinsonian disorderJessie C Jacobsen, Callum Wilson, Vicki Cunningham, et al.

Microarrays (Basel, Switzerland)|September 8, 2016

SNP Analysis and Whole Exome Sequencing: Their Application in the Analysis of a Consanguineous Pedigree Segregating AtaxiaSarah L Nickerson, Renate Marquis-Nicholson, Karen Claxton, et al.

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