Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M Anvret

Showing results (21-30 of 138) with videos related to

Pageof 14
Sort By:
Lakartidningen|March 11, 1992
[Neuromuscular diseases. Molecular genetic methods will revolutionize diagnosis and treatment]M Anvret, L Edström, G Ahlberg
Nucleic Acids Research|January 25, 1984
Evidence for integrated EBV genomes in Raji cellular DNAM Anvret, A Karlsson, G Bjursell
Neuromuscular Disorders : NMD|June 1, 1997
C4342T-mutation in the SCN4A gene on chromosome 17q in a Swedish family with paramyotonia congenita (Eulenburg)--correlations with clinical, neurophysiological and muscle biopsy dataK Borg, G Ahlberg, M Anvret
Lakartidningen|June 3, 1992
[Unstable DNA fragment can disclose carriers of dystrophia myotonica]M Anvret, K Johnson, L Edström
Human Genetics|February 1, 1994
WT1 mutations in patients with Denys-Drash syndrome: a novel mutation in exon 8 and paternal allele originA Nordenskjöld, E Friedman, M Anvret
Neurology|November 18, 1998
Larger CAG expansions in skeletal muscle compared with lymphocytes in Kennedy disease but not in Huntington diseaseT Ansved, A Lundin, M Anvret
Lakartidningen|February 5, 1997
[Development of molecular genetics and Charcot-Marie-Tooth disease. Important changes in clinical diagnostics]U Ericson, K Borg, M Anvret
Neuropediatrics|December 1, 1994
Rett syndrome: the bcl-2 gene--a mediator of neurotrophic mechanisms?M Anvret, Z P Zhang, B Hagberg
Human Genetics|February 1, 1990
Haplotyping of the human porphobilinogen deaminase gene in acute intermittent porphyria by polymerase chain reactionJ S Lee, J Lindsten, M Anvret
Journal of Pediatric Surgery|July 1, 1996
No evidence of WT1 gene mutations in children with congenital diaphragmatic herniaA Nordenskjöld, M Tapper-Persson, M Anvret
Pageof 14

Showing results (21-30 of 138) with videos related to

Sort By:
Pageof 14
Lakartidningen|March 11, 1992
[Neuromuscular diseases. Molecular genetic methods will revolutionize diagnosis and treatment]M Anvret, L Edström, G Ahlberg
Nucleic Acids Research|January 25, 1984
Evidence for integrated EBV genomes in Raji cellular DNAM Anvret, A Karlsson, G Bjursell
Neuromuscular Disorders : NMD|June 1, 1997
C4342T-mutation in the SCN4A gene on chromosome 17q in a Swedish family with paramyotonia congenita (Eulenburg)--correlations with clinical, neurophysiological and muscle biopsy dataK Borg, G Ahlberg, M Anvret
Lakartidningen|June 3, 1992
[Unstable DNA fragment can disclose carriers of dystrophia myotonica]M Anvret, K Johnson, L Edström
Human Genetics|February 1, 1994
WT1 mutations in patients with Denys-Drash syndrome: a novel mutation in exon 8 and paternal allele originA Nordenskjöld, E Friedman, M Anvret
Neurology|November 18, 1998
Larger CAG expansions in skeletal muscle compared with lymphocytes in Kennedy disease but not in Huntington diseaseT Ansved, A Lundin, M Anvret
Lakartidningen|February 5, 1997
[Development of molecular genetics and Charcot-Marie-Tooth disease. Important changes in clinical diagnostics]U Ericson, K Borg, M Anvret
Neuropediatrics|December 1, 1994
Rett syndrome: the bcl-2 gene--a mediator of neurotrophic mechanisms?M Anvret, Z P Zhang, B Hagberg
Human Genetics|February 1, 1990
Haplotyping of the human porphobilinogen deaminase gene in acute intermittent porphyria by polymerase chain reactionJ S Lee, J Lindsten, M Anvret
Journal of Pediatric Surgery|July 1, 1996
No evidence of WT1 gene mutations in children with congenital diaphragmatic herniaA Nordenskjöld, M Tapper-Persson, M Anvret
Pageof 14