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M Anvret

Showing results (81-90 of 138) with videos related to

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European Archives of Psychiatry and Clinical Neuroscience|January 1, 1994
Dopamine D1 receptor number--a sensitive PET marker for early brain degeneration in Huntington's diseaseG Sedvall, P Karlsson, A Lundin, et al.
Human Genetics|April 1, 1991
Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutationsN Archidiacono, M Lerone, M Rocchi, et al.
Human Genetics|January 1, 1990
A normal male with an inherited deletion of one exon within the DMD geneM Nordenskjöld, L Nicholson, L Edström, et al.
American Journal of Human Genetics|March 3, 1999
Autosomal dominant myopathy with proximal weakness and early respiratory muscle involvement maps to chromosome 2qP Nicolao, F Xiang, L G Gunnarsson, et al.
Human Genetics|August 1, 1991
Genetic heterogeneity of the porphobilinogen deaminase gene in Swedish families with acute intermittent porphyriaJ S Lee, G Lundin, L Lannfelt, et al.
American Journal of Medical Genetics|January 24, 1998
Reactions to predictive testing in Huntington disease: case reports of coping with a new genetic statusT B Wahlin, A Lundin, L Bäckman, et al.
The Journal of General Virology|December 1, 1991
B cell phenotype-dependent expression of the Epstein-Barr virus nuclear antigens EBNA-2 to EBNA-6: studies with somatic cell hybridsB A Contreras-Brodin, M Anvret, S Imreh, et al.
Clinical Genetics|May 20, 1999
Mutations in the endothelin-receptor B gene in Hirschsprung disease in SwedenP J Svensson, M Tapper-Persson, M Anvret, et al.
Urological Research|March 26, 1999
Screening for mutations in candidate genes for hypospadiasA Nordenskjöld, E Friedman, M Tapper-Persson, et al.
Lakartidningen|January 4, 1995
[Gene identification for Huntington's disease. Direkt mutational analysis confirms the diagnosis]E Almqvist, E Björck, J Wahlström, et al.
Pageof 14

Showing results (81-90 of 138) with videos related to

Sort By:
Pageof 14
European Archives of Psychiatry and Clinical Neuroscience|January 1, 1994
Dopamine D1 receptor number--a sensitive PET marker for early brain degeneration in Huntington's diseaseG Sedvall, P Karlsson, A Lundin, et al.
Human Genetics|April 1, 1991
Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutationsN Archidiacono, M Lerone, M Rocchi, et al.
Human Genetics|January 1, 1990
A normal male with an inherited deletion of one exon within the DMD geneM Nordenskjöld, L Nicholson, L Edström, et al.
American Journal of Human Genetics|March 3, 1999
Autosomal dominant myopathy with proximal weakness and early respiratory muscle involvement maps to chromosome 2qP Nicolao, F Xiang, L G Gunnarsson, et al.
Human Genetics|August 1, 1991
Genetic heterogeneity of the porphobilinogen deaminase gene in Swedish families with acute intermittent porphyriaJ S Lee, G Lundin, L Lannfelt, et al.
American Journal of Medical Genetics|January 24, 1998
Reactions to predictive testing in Huntington disease: case reports of coping with a new genetic statusT B Wahlin, A Lundin, L Bäckman, et al.
The Journal of General Virology|December 1, 1991
B cell phenotype-dependent expression of the Epstein-Barr virus nuclear antigens EBNA-2 to EBNA-6: studies with somatic cell hybridsB A Contreras-Brodin, M Anvret, S Imreh, et al.
Clinical Genetics|May 20, 1999
Mutations in the endothelin-receptor B gene in Hirschsprung disease in SwedenP J Svensson, M Tapper-Persson, M Anvret, et al.
Urological Research|March 26, 1999
Screening for mutations in candidate genes for hypospadiasA Nordenskjöld, E Friedman, M Tapper-Persson, et al.
Lakartidningen|January 4, 1995
[Gene identification for Huntington's disease. Direkt mutational analysis confirms the diagnosis]E Almqvist, E Björck, J Wahlström, et al.
Pageof 14