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Morten Duno

Showing results (1-10 of 108) with videos related to

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Rheumatology International|August 20, 2010
Molecular evaluation of 458 patients referred with a clinical diagnosis of familial Mediterranean fever in ScandinaviaNanna Cornelius, Morten Duno
Brain : a Journal of Neurology|February 1, 2017
Reply: Dominant LGMD2A: alternative diagnosis or hidden digenism?John Vissing, Morten Duno
Neuromuscular Disorders : NMD|January 30, 2013
ResponseNanna Witting, Morten Duno, John Vissing
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 24, 2012
Deletion of exon 26 of the dystrophin gene is associated with a mild Becker muscular dystrophy phenotypeNanna Witting, Morten Duno, John Vissing
Annals of Human Genetics|February 22, 2005
dHPLC screening of the NSD1 gene identifies nine novel mutations--summary of the first 100 Sotos syndrome mutationsLinea Melchior, Marianne Schwartz, Morten Duno
Prenatal Diagnosis|April 23, 2014
Fetal gender adjustment decreases the expected variance in non-invasive prenatal testing analysisPeter Johansen, Morten Duno, Susanne Kjaergaard
Frontiers in Genetics|November 2, 2020
Mutation Load of Single, Large-Scale Deletions of mtDNA in Mitotic and Postmitotic TissuesTina D Jeppesen, Morten Duno, John Vissing
Neurology|July 13, 2006
Autosomal dominant monosymptomatic myotonia permanensEskild Colding-Jørgensen, Morten Duno, John Vissing
European Journal of Neurology|August 4, 2025
Clinical and Genetic Reassessment in Patients With Clinically Diagnosed Hereditary PolyneuropathyLouise Sloth Kodal, Morten Duno, Tina Dysgaard
Annals of Human Genetics|May 28, 2009
High-resolution melting facilitates mutation screening of PYGM in patients with McArdle diseaseMorten Duno, Ros Quinlivan, John Vissing, et al.
Pageof 11

Showing results (1-10 of 108) with videos related to

Sort By:
Pageof 11
Rheumatology International|August 20, 2010
Molecular evaluation of 458 patients referred with a clinical diagnosis of familial Mediterranean fever in ScandinaviaNanna Cornelius, Morten Duno
Brain : a Journal of Neurology|February 1, 2017
Reply: Dominant LGMD2A: alternative diagnosis or hidden digenism?John Vissing, Morten Duno
Neuromuscular Disorders : NMD|January 30, 2013
ResponseNanna Witting, Morten Duno, John Vissing
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 24, 2012
Deletion of exon 26 of the dystrophin gene is associated with a mild Becker muscular dystrophy phenotypeNanna Witting, Morten Duno, John Vissing
Annals of Human Genetics|February 22, 2005
dHPLC screening of the NSD1 gene identifies nine novel mutations--summary of the first 100 Sotos syndrome mutationsLinea Melchior, Marianne Schwartz, Morten Duno
Prenatal Diagnosis|April 23, 2014
Fetal gender adjustment decreases the expected variance in non-invasive prenatal testing analysisPeter Johansen, Morten Duno, Susanne Kjaergaard
Frontiers in Genetics|November 2, 2020
Mutation Load of Single, Large-Scale Deletions of mtDNA in Mitotic and Postmitotic TissuesTina D Jeppesen, Morten Duno, John Vissing
Neurology|July 13, 2006
Autosomal dominant monosymptomatic myotonia permanensEskild Colding-Jørgensen, Morten Duno, John Vissing
European Journal of Neurology|August 4, 2025
Clinical and Genetic Reassessment in Patients With Clinically Diagnosed Hereditary PolyneuropathyLouise Sloth Kodal, Morten Duno, Tina Dysgaard
Annals of Human Genetics|May 28, 2009
High-resolution melting facilitates mutation screening of PYGM in patients with McArdle diseaseMorten Duno, Ros Quinlivan, John Vissing, et al.
Pageof 11