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S N Thibodeau

Showing results (41-50 of 156) with videos related to

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Gut|December 24, 1998
H63D is an haemochromatosis associated alleleV F Fairbanks, D J Brandhagen, S N Thibodeau, et al.
Human Molecular Genetics|September 1, 1994
Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutationK Snow, D J Tester, K E Kruckeberg, et al.
Biotechniques|March 26, 1999
Representative cDNA libraries and their utility in gene expression profilingW O Endege, K E Steinmann, L A Boardman, et al.
Nucleic Acids Research|April 29, 1998
Denaturing high performance liquid chromatography (DHPLC) used in the detection of germline and somatic mutationsW Liu, D I Smith, K J Rechtzigel, et al.
Journal of Medical Genetics|November 1, 1995
Exclusion of a primary gene defect at the HLA locus in familial idiopathic dilated cardiomyopathyT M Olson, S N Thibodeau, P A Lundquist, et al.
Annals of the New York Academy of Sciences|December 16, 1996
Predictive value of APOE genotyping in incipient Alzheimer's diseaseR C Petersen, S C Waring, G E Smith, et al.
Mayo Clinic Proceedings|May 1, 1990
Confirmation of lymphomatous pulmonary involvement by immunophenotypic and gene rearrangement analysis of bronchoalveolar lavage fluidR J Pisani, T E Witzig, C Y Li, et al.
Hemoglobin|March 11, 1998
DNA sequence analysis proves Hb M-Milwaukee-2 is due to beta-globin gene codon 92 (CAC-->TAC), the presumed mutation of Hb M-Hyde Park and Hb M-AkitaP J Hutt, A V Pisciotta, V F Fairbanks, et al.
American Journal of Medical Genetics|April 1, 1992
Linkage of nonspecific X-linked mental retardation to Xq21.31K B Jedele, V V Michels, D J Schaid, et al.
American Journal of Medical Genetics|March 15, 1994
Screening the dystrophin gene suggests a high rate of polymorphism in general but no exonic deletions in schizophrenicsN M Lindor, J L Sobell, L L Heston, et al.
Pageof 16

Showing results (41-50 of 156) with videos related to

Sort By:
Pageof 16
Gut|December 24, 1998
H63D is an haemochromatosis associated alleleV F Fairbanks, D J Brandhagen, S N Thibodeau, et al.
Human Molecular Genetics|September 1, 1994
Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutationK Snow, D J Tester, K E Kruckeberg, et al.
Biotechniques|March 26, 1999
Representative cDNA libraries and their utility in gene expression profilingW O Endege, K E Steinmann, L A Boardman, et al.
Nucleic Acids Research|April 29, 1998
Denaturing high performance liquid chromatography (DHPLC) used in the detection of germline and somatic mutationsW Liu, D I Smith, K J Rechtzigel, et al.
Journal of Medical Genetics|November 1, 1995
Exclusion of a primary gene defect at the HLA locus in familial idiopathic dilated cardiomyopathyT M Olson, S N Thibodeau, P A Lundquist, et al.
Annals of the New York Academy of Sciences|December 16, 1996
Predictive value of APOE genotyping in incipient Alzheimer's diseaseR C Petersen, S C Waring, G E Smith, et al.
Mayo Clinic Proceedings|May 1, 1990
Confirmation of lymphomatous pulmonary involvement by immunophenotypic and gene rearrangement analysis of bronchoalveolar lavage fluidR J Pisani, T E Witzig, C Y Li, et al.
Hemoglobin|March 11, 1998
DNA sequence analysis proves Hb M-Milwaukee-2 is due to beta-globin gene codon 92 (CAC-->TAC), the presumed mutation of Hb M-Hyde Park and Hb M-AkitaP J Hutt, A V Pisciotta, V F Fairbanks, et al.
American Journal of Medical Genetics|April 1, 1992
Linkage of nonspecific X-linked mental retardation to Xq21.31K B Jedele, V V Michels, D J Schaid, et al.
American Journal of Medical Genetics|March 15, 1994
Screening the dystrophin gene suggests a high rate of polymorphism in general but no exonic deletions in schizophrenicsN M Lindor, J L Sobell, L L Heston, et al.
Pageof 16