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M Anvret

Showing results (11-20 of 138) with videos related to

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Nucleic Acids Research|April 11, 1989
An EcoRI polymorphism of the human von Willebrand factor cDNA (VWF)M Lindstedt, M Anvret
Neuropediatrics|April 1, 1995
Current status of genetic research in Rett syndromeM Anvret, Z P Zhang
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1991
Identification of the most common mutation within the porphobilinogen deaminase gene in Swedish patients with acute intermittent porphyriaJ S Lee, M Anvret
Nucleic Acids Research|August 11, 1987
A PstI polymorphism for the human porphobilinogen deaminase gene (PBG)J S Lee, M Anvret
Nucleic Acids Research|March 11, 1989
PstI RFLP for the anonymous [D13S2] (p9D11) probeJ S Lee, M Anvret
Lakartidningen|May 19, 1993
[Huntington's disease. The elusive "gene" is now identified]M Anvret, G Holmgren, J Wahlström
Clinical Genetics|June 26, 2002
MECP2 mutations in Swedish Rett syndrome clustersF Xiang, Y Stenbom, M Anvret
Human Genetics|July 1, 1995
Absence of mutations in the WT1 gene in patients with XY gonadal dysgenesisA Nordenskjöld, G Fricke, M Anvret
European Journal of Neurology|April 22, 1999
CTG-repeat length in distal and proximal leg muscles of symptomatic and non-symptomatic patients with myotonic dystrophy: relation to muscle strength and degree of histopathological abnormalitiesB Hedberg, M Anvret, T Ansved
Journal of Internal Medicine. Supplement|January 1, 1997
Understanding von Willebrand's disease from gene defects to the patientsZ Zhang, M Blombäck, M Anvret
Pageof 14

Showing results (11-20 of 138) with videos related to

Sort By:
Pageof 14
Nucleic Acids Research|April 11, 1989
An EcoRI polymorphism of the human von Willebrand factor cDNA (VWF)M Lindstedt, M Anvret
Neuropediatrics|April 1, 1995
Current status of genetic research in Rett syndromeM Anvret, Z P Zhang
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1991
Identification of the most common mutation within the porphobilinogen deaminase gene in Swedish patients with acute intermittent porphyriaJ S Lee, M Anvret
Nucleic Acids Research|August 11, 1987
A PstI polymorphism for the human porphobilinogen deaminase gene (PBG)J S Lee, M Anvret
Nucleic Acids Research|March 11, 1989
PstI RFLP for the anonymous [D13S2] (p9D11) probeJ S Lee, M Anvret
Lakartidningen|May 19, 1993
[Huntington's disease. The elusive "gene" is now identified]M Anvret, G Holmgren, J Wahlström
Clinical Genetics|June 26, 2002
MECP2 mutations in Swedish Rett syndrome clustersF Xiang, Y Stenbom, M Anvret
Human Genetics|July 1, 1995
Absence of mutations in the WT1 gene in patients with XY gonadal dysgenesisA Nordenskjöld, G Fricke, M Anvret
European Journal of Neurology|April 22, 1999
CTG-repeat length in distal and proximal leg muscles of symptomatic and non-symptomatic patients with myotonic dystrophy: relation to muscle strength and degree of histopathological abnormalitiesB Hedberg, M Anvret, T Ansved
Journal of Internal Medicine. Supplement|January 1, 1997
Understanding von Willebrand's disease from gene defects to the patientsZ Zhang, M Blombäck, M Anvret
Pageof 14