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M Anvret

Showing results (101-110 of 138) with videos related to

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Human Genetics|February 1, 1994
394delTT: a Nordic cystic fibrosis mutationM Schwartz, M Anvret, M Claustres, et al.
Lakartidningen|November 22, 1989
[Rett syndrome--from a healthy infant to a disabled woman]J Wahlström, B Hagberg, M Anvret, et al.
American Journal of Human Genetics|October 11, 2001
Huntington disease phenocopy is a familial prion diseaseR C Moore, F Xiang, J Monaghan, et al.
Journal of Medical Genetics|December 1, 1995
Four mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyriaG Lundin, J Hashemi, Y Floderus, et al.
Journal of Internal Medicine|March 1, 1995
Diagnosis of acute intermittent porphyria in northern Sweden: an evaluation of mutation analysis and biochemical methodsC Andersson, S Thunell, Y Floderus, et al.
American Journal of Human Genetics|October 30, 1998
A Huntington disease-like neurodegenerative disorder maps to chromosome 20pF Xiang, E W Almqvist, M Huq, et al.
Genomics|November 1, 1989
Recombination events that locate myotonic dystrophy distal to APOC2 on 19qK Johnson, P Shelbourne, J Davies, et al.
Journal of Virology|October 9, 1999
The trophoblastic epithelial barrier is not infected in full-term placentae of human immunodeficiency virus-seropositive mothers undergoing antiretroviral therapyC Tscherning-Casper, N Papadogiannakis, M Anvret, et al.
European Journal of Cancer & Clinical Oncology|October 1, 1983
Epstein-Barr virus markers in a series of Burkitt's lymphomas from the West Nile District, UgandaA Geser, G M Lenoir, M Anvret, et al.
British Medical Journal (Clinical Research Ed.)|February 7, 1981
Epstein-Barr-virus-carrying lymphoma in a patient with ataxia-telangiectasiaA K Saemundsen, A I Berkel, W Henle, et al.
Pageof 14

Showing results (101-110 of 138) with videos related to

Sort By:
Pageof 14
Human Genetics|February 1, 1994
394delTT: a Nordic cystic fibrosis mutationM Schwartz, M Anvret, M Claustres, et al.
Lakartidningen|November 22, 1989
[Rett syndrome--from a healthy infant to a disabled woman]J Wahlström, B Hagberg, M Anvret, et al.
American Journal of Human Genetics|October 11, 2001
Huntington disease phenocopy is a familial prion diseaseR C Moore, F Xiang, J Monaghan, et al.
Journal of Medical Genetics|December 1, 1995
Four mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyriaG Lundin, J Hashemi, Y Floderus, et al.
Journal of Internal Medicine|March 1, 1995
Diagnosis of acute intermittent porphyria in northern Sweden: an evaluation of mutation analysis and biochemical methodsC Andersson, S Thunell, Y Floderus, et al.
American Journal of Human Genetics|October 30, 1998
A Huntington disease-like neurodegenerative disorder maps to chromosome 20pF Xiang, E W Almqvist, M Huq, et al.
Genomics|November 1, 1989
Recombination events that locate myotonic dystrophy distal to APOC2 on 19qK Johnson, P Shelbourne, J Davies, et al.
Journal of Virology|October 9, 1999
The trophoblastic epithelial barrier is not infected in full-term placentae of human immunodeficiency virus-seropositive mothers undergoing antiretroviral therapyC Tscherning-Casper, N Papadogiannakis, M Anvret, et al.
European Journal of Cancer & Clinical Oncology|October 1, 1983
Epstein-Barr virus markers in a series of Burkitt's lymphomas from the West Nile District, UgandaA Geser, G M Lenoir, M Anvret, et al.
British Medical Journal (Clinical Research Ed.)|February 7, 1981
Epstein-Barr-virus-carrying lymphoma in a patient with ataxia-telangiectasiaA K Saemundsen, A I Berkel, W Henle, et al.
Pageof 14