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S N Thibodeau

Showing results (51-60 of 156) with videos related to

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Human Genetics|March 1, 1995
Transthyretin Ser 6 gene frequency in individuals without amyloidosisD R Jacobson, I L Alves, M J Saraiva, et al.
Science (New York, N.Y.)|May 23, 1998
Actin mutations in dilated cardiomyopathy, a heritable form of heart failureT M Olson, V V Michels, S N Thibodeau, et al.
American Journal of Medical Genetics|July 15, 1994
Reliability of diagnostic assessment of normal and premutation status in the fragile X syndrome using DNA testingG S Fisch, D L Nelson, K Snow, et al.
Human Genetics|April 6, 1999
Supravalvular aortic stenosis: a splice site mutation within the elastin gene results in reduced expression of two aberrantly spliced transcriptsZ Urbán, V V Michels, S N Thibodeau, et al.
Cancer|September 15, 1992
Current status of adjuvant chemotherapy for colorectal cancer. Can molecular markers play a role in predicting prognosis?M J O'Connell, D J Schaid, V Ganju, et al.
American Journal of Human Genetics|December 1, 1993
Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general populationK Snow, L K Doud, R Hagerman, et al.
Hemoglobin|March 11, 1998
Hb Tak confirmed by DNA analysis: not expressed as thalassemia in a Hb Tak/Hb E compound heterozygoteJ D Hoyer, M J Wick, S N Thibodeau, et al.
Leukemia|December 1, 1990
The location of the Philadelphia chromosomal breakpoint site and prognosis in chronic granulocytic leukemiaA Tefferi, G D Bren, K V Wagner, et al.
International Journal of Oncology|December 22, 1999
Differential expression and allelotyping of the p73 gene in neuroblastomaW Liu, M Mai, A Yokomizo, et al.
Cancer|December 26, 2001
DNA mismatch repair genes hMLH1, hMSH2, and hMSH6 are not inactivated in bronchioloalveolar carcinomas of the lungM C Aubry, K C Halling, J L Myers, et al.
Pageof 16

Showing results (51-60 of 156) with videos related to

Sort By:
Pageof 16
Human Genetics|March 1, 1995
Transthyretin Ser 6 gene frequency in individuals without amyloidosisD R Jacobson, I L Alves, M J Saraiva, et al.
Science (New York, N.Y.)|May 23, 1998
Actin mutations in dilated cardiomyopathy, a heritable form of heart failureT M Olson, V V Michels, S N Thibodeau, et al.
American Journal of Medical Genetics|July 15, 1994
Reliability of diagnostic assessment of normal and premutation status in the fragile X syndrome using DNA testingG S Fisch, D L Nelson, K Snow, et al.
Human Genetics|April 6, 1999
Supravalvular aortic stenosis: a splice site mutation within the elastin gene results in reduced expression of two aberrantly spliced transcriptsZ Urbán, V V Michels, S N Thibodeau, et al.
Cancer|September 15, 1992
Current status of adjuvant chemotherapy for colorectal cancer. Can molecular markers play a role in predicting prognosis?M J O'Connell, D J Schaid, V Ganju, et al.
American Journal of Human Genetics|December 1, 1993
Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general populationK Snow, L K Doud, R Hagerman, et al.
Hemoglobin|March 11, 1998
Hb Tak confirmed by DNA analysis: not expressed as thalassemia in a Hb Tak/Hb E compound heterozygoteJ D Hoyer, M J Wick, S N Thibodeau, et al.
Leukemia|December 1, 1990
The location of the Philadelphia chromosomal breakpoint site and prognosis in chronic granulocytic leukemiaA Tefferi, G D Bren, K V Wagner, et al.
International Journal of Oncology|December 22, 1999
Differential expression and allelotyping of the p73 gene in neuroblastomaW Liu, M Mai, A Yokomizo, et al.
Cancer|December 26, 2001
DNA mismatch repair genes hMLH1, hMSH2, and hMSH6 are not inactivated in bronchioloalveolar carcinomas of the lungM C Aubry, K C Halling, J L Myers, et al.
Pageof 16