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T W Prior

Showing results (51-60 of 75) with videos related to

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Nature Genetics|August 1, 1993
A missense mutation in the dystrophin gene in a Duchenne muscular dystrophy patientT W Prior, A C Papp, P J Snyder, et al.
Neurology|August 29, 2001
Diagnosis of Duchenne dystrophy by enhanced detection of small mutationsJ R Mendell, C H Buzin, J Feng, et al.
American Journal of Human Genetics|July 1, 1995
Spectrum of small mutations in the dystrophin coding regionT W Prior, C Bartolo, D K Pearl, et al.
Human Mutation|January 1, 1993
Exon 44 nonsense mutation in two-Duchenne muscular dystrophy brothers detected by heteroduplex analysisT W Prior, A C Papp, P J Snyder, et al.
American Journal of Human Genetics|June 1, 1997
Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy numberP E McAndrew, D W Parsons, L R Simard, et al.
Neurogenetics|March 25, 2000
Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7C F Rochette, L C Surh, P N Ray, et al.
Human Mutation|January 1, 1995
Rapid DNA haplotyping using a multiplex heteroduplex approach: application to Duchenne muscular dystrophy carrier testingT W Prior, G D Wenger, A C Papp, et al.
Clinical Chemistry|January 1, 1995
A molecular protocol for diagnosing myotonic dystrophyM Guida, R S Marger, A C Papp, et al.
Transplantation|June 27, 1994
Detection of cytomegalovirus in liver transplant biopsies. A comparison of light microscopy, immunohistochemistry, duplex PCR and nested PCRJ A Brainard, J K Greenson, C J Vesy, et al.
Genetic Testing|January 1, 1997
Methylation analysis of the fragile X syndrome by PCRS Das, T Kubota, M Song, et al.
Pageof 8

Showing results (51-60 of 75) with videos related to

Sort By:
Pageof 8
Nature Genetics|August 1, 1993
A missense mutation in the dystrophin gene in a Duchenne muscular dystrophy patientT W Prior, A C Papp, P J Snyder, et al.
Neurology|August 29, 2001
Diagnosis of Duchenne dystrophy by enhanced detection of small mutationsJ R Mendell, C H Buzin, J Feng, et al.
American Journal of Human Genetics|July 1, 1995
Spectrum of small mutations in the dystrophin coding regionT W Prior, C Bartolo, D K Pearl, et al.
Human Mutation|January 1, 1993
Exon 44 nonsense mutation in two-Duchenne muscular dystrophy brothers detected by heteroduplex analysisT W Prior, A C Papp, P J Snyder, et al.
American Journal of Human Genetics|June 1, 1997
Identification of proximal spinal muscular atrophy carriers and patients by analysis of SMNT and SMNC gene copy numberP E McAndrew, D W Parsons, L R Simard, et al.
Neurogenetics|March 25, 2000
Molecular diagnosis of non-deletion SMA patients using quantitative PCR of SMN exon 7C F Rochette, L C Surh, P N Ray, et al.
Human Mutation|January 1, 1995
Rapid DNA haplotyping using a multiplex heteroduplex approach: application to Duchenne muscular dystrophy carrier testingT W Prior, G D Wenger, A C Papp, et al.
Clinical Chemistry|January 1, 1995
A molecular protocol for diagnosing myotonic dystrophyM Guida, R S Marger, A C Papp, et al.
Transplantation|June 27, 1994
Detection of cytomegalovirus in liver transplant biopsies. A comparison of light microscopy, immunohistochemistry, duplex PCR and nested PCRJ A Brainard, J K Greenson, C J Vesy, et al.
Genetic Testing|January 1, 1997
Methylation analysis of the fragile X syndrome by PCRS Das, T Kubota, M Song, et al.
Pageof 8