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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Catarina Lundin

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Journal of Hematology & Oncology|April 15, 2014

Clinical and genetic features of pediatric acute lymphoblastic leukemia in Down syndrome in the Nordic countriesCatarina Lundin, Erik Forestier, Mette Klarskov Andersen, et al.

Heart Rhythm|March 25, 2026

Genotype-phenotype correlation of 139 p.Gln530Ter-KCNQ1 patients with inherited long QT syndromeAleksei Savelev, Nina Larsson, Pia Dahlberg, et al.

European Journal of Human Genetics : EJHG|July 14, 2016

Rare novel variants in the ZIC3 gene cause X-linked heterotaxyAimee D C Paulussen, Anja Steyls, Jo Vanoevelen, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 7, 2020

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controlsRoddy Walsh, Najim Lahrouchi, Rafik Tadros, et al.

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Search research articles

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 Hematology & Oncology|April 15, 2014

Clinical and genetic features of pediatric acute lymphoblastic leukemia in Down syndrome in the Nordic countriesCatarina Lundin, Erik Forestier, Mette Klarskov Andersen, et al.

Heart Rhythm|March 25, 2026

Genotype-phenotype correlation of 139 p.Gln530Ter-KCNQ1 patients with inherited long QT syndromeAleksei Savelev, Nina Larsson, Pia Dahlberg, et al.

European Journal of Human Genetics : EJHG|July 14, 2016

Rare novel variants in the ZIC3 gene cause X-linked heterotaxyAimee D C Paulussen, Anja Steyls, Jo Vanoevelen, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 7, 2020

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controlsRoddy Walsh, Najim Lahrouchi, Rafik Tadros, et al.

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