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Morten Dunø

Showing results (1-10 of 67) with videos related to

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Genetic Testing|February 3, 2005
Improved molecular diagnosis of dystrophin gene mutations using the multiplex ligation-dependent probe amplification methodMarianne Schwartz, Morten Dunø
Muscle & Nerve|March 28, 2003
Decrement of compound muscle action potential is related to mutation type in myotonia congenitaEskild Colding-Jørgensen, Morten DunØ, Marianne Schwartz, et al.
Clinical Dysmorphology|March 2, 2016
Monozygotic twins presenting with isolated sagittal and bicoronal synostosis, respectivelyHanne D Hove, Morten Dunø, Per Larsen, et al.
Neurology|August 23, 2006
Do carriers of PYGM mutations have symptoms of McArdle disease?Susanne Tvede Andersen, Morten Dunø, Marianne Schwartz, et al.
Ugeskrift for Laeger|October 30, 2014
[Genetic counselling is relevant in familial as well as sporadic cases of amyotrophic lateral sclerosis]Suzanne Granhøj Lindquist, Morten Dunø, Kirsten Svenstrup, et al.
Human Genetics|September 21, 2004
Mapping genomic deletions down to the base: a quantitative copy number scanning approach used to characterise and clone the breakpoints of a recurrent 7p14.2p15.3 deletionMorten Dunø, Hanne Hove, Maria Kirchhoff, et al.
American Journal of Medical Genetics. Part A|April 7, 2022
Novel truncating variants in FGD1 detected in two Danish families with Aarskog-Scott syndrome and myopathic featuresAllan Bayat, Bjørg Krett, Morten Dunø, et al.
The Journal of Clinical Endocrinology and Metabolism|July 12, 2019
Hydroxylated Long-Chain Acylcarnitines are Biomarkers of Mitochondrial MyopathyChristoffer Rasmus Vissing, Morten Dunø, Flemming Wibrand, et al.
Genes|August 23, 2020
Stable Longitudinal Methylation Levels at the CpG Sites Flanking the CTG Repeat of <i>DMPK</i> in Patients with Myotonic Dystrophy Type 1Mathis Hildonen, Kirsten Lykke Knak, Morten Dunø, et al.
Human Mutation|January 18, 2007
Deletion of exon 16 of the dystrophin gene is not associated with diseaseMarianne Schwartz, Morten Dunø, Anne Lise Palle, et al.
Pageof 7

Showing results (1-10 of 67) with videos related to

Sort By:
Pageof 7
Genetic Testing|February 3, 2005
Improved molecular diagnosis of dystrophin gene mutations using the multiplex ligation-dependent probe amplification methodMarianne Schwartz, Morten Dunø
Muscle & Nerve|March 28, 2003
Decrement of compound muscle action potential is related to mutation type in myotonia congenitaEskild Colding-Jørgensen, Morten DunØ, Marianne Schwartz, et al.
Clinical Dysmorphology|March 2, 2016
Monozygotic twins presenting with isolated sagittal and bicoronal synostosis, respectivelyHanne D Hove, Morten Dunø, Per Larsen, et al.
Neurology|August 23, 2006
Do carriers of PYGM mutations have symptoms of McArdle disease?Susanne Tvede Andersen, Morten Dunø, Marianne Schwartz, et al.
Ugeskrift for Laeger|October 30, 2014
[Genetic counselling is relevant in familial as well as sporadic cases of amyotrophic lateral sclerosis]Suzanne Granhøj Lindquist, Morten Dunø, Kirsten Svenstrup, et al.
Human Genetics|September 21, 2004
Mapping genomic deletions down to the base: a quantitative copy number scanning approach used to characterise and clone the breakpoints of a recurrent 7p14.2p15.3 deletionMorten Dunø, Hanne Hove, Maria Kirchhoff, et al.
American Journal of Medical Genetics. Part A|April 7, 2022
Novel truncating variants in FGD1 detected in two Danish families with Aarskog-Scott syndrome and myopathic featuresAllan Bayat, Bjørg Krett, Morten Dunø, et al.
The Journal of Clinical Endocrinology and Metabolism|July 12, 2019
Hydroxylated Long-Chain Acylcarnitines are Biomarkers of Mitochondrial MyopathyChristoffer Rasmus Vissing, Morten Dunø, Flemming Wibrand, et al.
Genes|August 23, 2020
Stable Longitudinal Methylation Levels at the CpG Sites Flanking the CTG Repeat of <i>DMPK</i> in Patients with Myotonic Dystrophy Type 1Mathis Hildonen, Kirsten Lykke Knak, Morten Dunø, et al.
Human Mutation|January 18, 2007
Deletion of exon 16 of the dystrophin gene is not associated with diseaseMarianne Schwartz, Morten Dunø, Anne Lise Palle, et al.
Pageof 7