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M Anvret

Showing results (41-50 of 138) with videos related to

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Biochemical and Biophysical Research Communications|March 10, 2001
A mammalian radial spokehead-like gene, RSHL1, at the myotonic dystrophy-1 locusM Eriksson, T Ansved, M Anvret, et al.
American Journal of Medical Genetics|September 1, 1990
Segregation analysis of the X-chromosome in a family with Rett syndrome in two generationsM Anvret, J Wahlström, P Skogsberg, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 2, 1998
A new approach to gene therapyZ Zhang, M Eriksson, M Blombäck, et al.
Human Genetics|October 1, 1995
Effects of the mutant von Willebrand factor gene in von Willebrand diseaseZ Zhang, M Lindstedt, M Blombäck, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1993
Mutations of von Willebrand factor gene in families with von Willebrand disease in the Aland IslandsZ P Zhang, M Blombäck, D Nyman, et al.
Brain & Development|January 1, 1985
Linkage analysis of the Rett syndrome using human chromosomal specific probesM Anvret, I M Johansson, J Wahlström, et al.
Human Genetics|July 1, 1997
Genetic investigation of the porphobilinogen deaminase gene in Swedish acute intermittent porphyria familiesG Lundin, J S Lee, S Thunell, et al.
Nature|November 29, 1990
A human XY female with a frame shift mutation in the candidate testis-determining gene SRYR J Jäger, M Anvret, K Hall, et al.
Human Molecular Genetics|May 20, 1999
Simultaneous analysis of expression of the three myotonic dystrophy locus genes in adult skeletal muscle samples: the CTG expansion correlates inversely with DMPK and 59 expression levels, but not DMAHP levelsM Eriksson, T Ansved, L Edström, et al.
International Journal of Cancer|November 15, 1995
Constitutional and somatic mutations in the WT1 gene in Wilms' tumor patientsA Nordenskjöld, E Friedman, B Sandstedt, et al.
Pageof 14

Showing results (41-50 of 138) with videos related to

Sort By:
Pageof 14
Biochemical and Biophysical Research Communications|March 10, 2001
A mammalian radial spokehead-like gene, RSHL1, at the myotonic dystrophy-1 locusM Eriksson, T Ansved, M Anvret, et al.
American Journal of Medical Genetics|September 1, 1990
Segregation analysis of the X-chromosome in a family with Rett syndrome in two generationsM Anvret, J Wahlström, P Skogsberg, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 2, 1998
A new approach to gene therapyZ Zhang, M Eriksson, M Blombäck, et al.
Human Genetics|October 1, 1995
Effects of the mutant von Willebrand factor gene in von Willebrand diseaseZ Zhang, M Lindstedt, M Blombäck, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1993
Mutations of von Willebrand factor gene in families with von Willebrand disease in the Aland IslandsZ P Zhang, M Blombäck, D Nyman, et al.
Brain & Development|January 1, 1985
Linkage analysis of the Rett syndrome using human chromosomal specific probesM Anvret, I M Johansson, J Wahlström, et al.
Human Genetics|July 1, 1997
Genetic investigation of the porphobilinogen deaminase gene in Swedish acute intermittent porphyria familiesG Lundin, J S Lee, S Thunell, et al.
Nature|November 29, 1990
A human XY female with a frame shift mutation in the candidate testis-determining gene SRYR J Jäger, M Anvret, K Hall, et al.
Human Molecular Genetics|May 20, 1999
Simultaneous analysis of expression of the three myotonic dystrophy locus genes in adult skeletal muscle samples: the CTG expansion correlates inversely with DMPK and 59 expression levels, but not DMAHP levelsM Eriksson, T Ansved, L Edström, et al.
International Journal of Cancer|November 15, 1995
Constitutional and somatic mutations in the WT1 gene in Wilms' tumor patientsA Nordenskjöld, E Friedman, B Sandstedt, et al.
Pageof 14