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Arvid Heiberg

Showing results (21-30 of 35) with videos related to

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Acta Ophthalmologica Scandinavica|March 23, 2007
Ocular findings in Norwegian patients with ataxia-telangiectasia: a 5 year prospective cohort studyRuth Riise, Jan Ygge, Carl Lindman, et al.
Psychiatric Genetics|February 12, 2016
Parents' attitudes toward genetic research in autism spectrum disorderJarle Johannessen, Terje Nærland, Cinnamon Bloss, et al.
Neuromuscular Disorders : NMD|April 6, 2012
Hereditary motor neuron disease in a large Norwegian family with a "H46R" substitution in the superoxide dismutase 1 geneRune Østern, Toril Fagerheim, Kristin Ørstavik, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|April 23, 2024
Myotonic dystrophy type 1 - a multiorgan disorderKristin Ørstavik, Gro Solbakken, Magnhild Rasmussen, et al.
European Journal of Human Genetics : EJHG|September 5, 2013
Occipital horn syndrome and classical Menkes Syndrome caused by deep intronic mutations, leading to the activation of ATP7A pseudo-exonSaiqa Yasmeen, Katrine Lund, Anne De Paepe, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|May 13, 2024
Kristin Ørstavik, Gro Solbakken, Magnhild Rasmussen, et al.
American Journal of Medical Genetics. Part A|April 4, 2017
Neurofibromatosis type 2: Multiple intra-dermal tumors in a toddlerCecilie F Rustad, Hilde M Dahl, Naomi L Bowers, et al.
International Journal of Molecular Sciences|May 20, 2017
Parents' Attitudes toward Clinical Genetic Testing for Autism Spectrum Disorder-Data from a Norwegian SampleJarle Johannessen, Terje Nærland, Sigrun Hope, et al.
American Journal of Medical Genetics. Part A|November 23, 2011
Vestibular schwannomas occur in schwannomatosis and should not be considered an exclusion criterion for clinical diagnosisMiriam J Smith, Anjana Kulkarni, Cecilie Rustad, et al.
Heart (British Cardiac Society)|July 18, 2014
Familial globotriaosylceramide-associated cardiomyopathy mimicking Fabry diseaseTurid Apelland, Einar Gude, Erik H Strøm, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Acta Ophthalmologica Scandinavica|March 23, 2007
Ocular findings in Norwegian patients with ataxia-telangiectasia: a 5 year prospective cohort studyRuth Riise, Jan Ygge, Carl Lindman, et al.
Psychiatric Genetics|February 12, 2016
Parents' attitudes toward genetic research in autism spectrum disorderJarle Johannessen, Terje Nærland, Cinnamon Bloss, et al.
Neuromuscular Disorders : NMD|April 6, 2012
Hereditary motor neuron disease in a large Norwegian family with a "H46R" substitution in the superoxide dismutase 1 geneRune Østern, Toril Fagerheim, Kristin Ørstavik, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|April 23, 2024
Myotonic dystrophy type 1 - a multiorgan disorderKristin Ørstavik, Gro Solbakken, Magnhild Rasmussen, et al.
European Journal of Human Genetics : EJHG|September 5, 2013
Occipital horn syndrome and classical Menkes Syndrome caused by deep intronic mutations, leading to the activation of ATP7A pseudo-exonSaiqa Yasmeen, Katrine Lund, Anne De Paepe, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|May 13, 2024
Kristin Ørstavik, Gro Solbakken, Magnhild Rasmussen, et al.
American Journal of Medical Genetics. Part A|April 4, 2017
Neurofibromatosis type 2: Multiple intra-dermal tumors in a toddlerCecilie F Rustad, Hilde M Dahl, Naomi L Bowers, et al.
International Journal of Molecular Sciences|May 20, 2017
Parents' Attitudes toward Clinical Genetic Testing for Autism Spectrum Disorder-Data from a Norwegian SampleJarle Johannessen, Terje Nærland, Sigrun Hope, et al.
American Journal of Medical Genetics. Part A|November 23, 2011
Vestibular schwannomas occur in schwannomatosis and should not be considered an exclusion criterion for clinical diagnosisMiriam J Smith, Anjana Kulkarni, Cecilie Rustad, et al.
Heart (British Cardiac Society)|July 18, 2014
Familial globotriaosylceramide-associated cardiomyopathy mimicking Fabry diseaseTurid Apelland, Einar Gude, Erik H Strøm, et al.
Pageof 4