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T W Prior

Showing results (41-50 of 75) with videos related to

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Archives of Pathology & Laboratory Medicine|July 23, 1998
Differential diagnosis of hereditary hemochromatosis from other liver disorders by genetic analysis: gene mutation analysis of patients previously diagnosed with hemochromatosis by liver biopsyC Bartolo, P E McAndrew, R C Sosolik, et al.
Human Mutation|January 1, 1996
Nonsense mutations in a Becker muscular dystrophy and an intermediate patientT W Prior, C Bartolo, A C Papp, et al.
Human Molecular Genetics|July 1, 1994
Identification of a missense mutation, single base deletion and a polymorphism in the dystrophin exon 16T W Prior, C Bartolo, A C Papp, et al.
Human Molecular Genetics|June 17, 1999
A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2U R Monani, C L Lorson, D W Parsons, et al.
Clinical Genetics|April 16, 2003
Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2R E Pyatt, H Nakagawa, H Hampel, et al.
Annals of Neurology|February 1, 1997
Deletion and conversion in spinal muscular atrophy patients: is there a relationship to severity?C J DiDonato, S E Ingraham, J R Mendell, et al.
American Journal of Clinical Pathology|May 9, 2000
Transfusion-associated graft-vs-host disease. A fatal case caused by blood from an unrelated HLA homozygous donorT E Gorman, C J Julius, R F Barth, et al.
Journal of Medical Genetics|April 1, 1996
A novel splice site mutation in a Becker muscular dystrophy patientC Bartolo, A C Papp, P J Snyder, et al.
American Journal of Medical Genetics|March 1, 1994
Heteroduplex analysis of the dystrophin gene: application to point mutation and carrier detectionT W Prior, A C Papp, P J Snyder, et al.
Human Molecular Genetics|March 1, 1993
Identification of two point mutations and a one base deletion in exon 19 of the dystrophin gene by heteroduplex formationT W Prior, A C Papp, P J Snyder, et al.
Pageof 8

Showing results (41-50 of 75) with videos related to

Sort By:
Pageof 8
Archives of Pathology & Laboratory Medicine|July 23, 1998
Differential diagnosis of hereditary hemochromatosis from other liver disorders by genetic analysis: gene mutation analysis of patients previously diagnosed with hemochromatosis by liver biopsyC Bartolo, P E McAndrew, R C Sosolik, et al.
Human Mutation|January 1, 1996
Nonsense mutations in a Becker muscular dystrophy and an intermediate patientT W Prior, C Bartolo, A C Papp, et al.
Human Molecular Genetics|July 1, 1994
Identification of a missense mutation, single base deletion and a polymorphism in the dystrophin exon 16T W Prior, C Bartolo, A C Papp, et al.
Human Molecular Genetics|June 17, 1999
A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2U R Monani, C L Lorson, D W Parsons, et al.
Clinical Genetics|April 16, 2003
Identification of a deletion in the mismatch repair gene, MSH2, using mouse-human cell hybrids monosomal for chromosome 2R E Pyatt, H Nakagawa, H Hampel, et al.
Annals of Neurology|February 1, 1997
Deletion and conversion in spinal muscular atrophy patients: is there a relationship to severity?C J DiDonato, S E Ingraham, J R Mendell, et al.
American Journal of Clinical Pathology|May 9, 2000
Transfusion-associated graft-vs-host disease. A fatal case caused by blood from an unrelated HLA homozygous donorT E Gorman, C J Julius, R F Barth, et al.
Journal of Medical Genetics|April 1, 1996
A novel splice site mutation in a Becker muscular dystrophy patientC Bartolo, A C Papp, P J Snyder, et al.
American Journal of Medical Genetics|March 1, 1994
Heteroduplex analysis of the dystrophin gene: application to point mutation and carrier detectionT W Prior, A C Papp, P J Snyder, et al.
Human Molecular Genetics|March 1, 1993
Identification of two point mutations and a one base deletion in exon 19 of the dystrophin gene by heteroduplex formationT W Prior, A C Papp, P J Snyder, et al.
Pageof 8