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Thomas W Prior

Showing results (11-20 of 82) with videos related to

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The Journal of Molecular Diagnostics : JMD|July 29, 2005
Experience and strategy for the molecular testing of Duchenne muscular dystrophyThomas W Prior, Scott J Bridgeman
Current Protocols in Human Genetics|January 12, 2010
Identifying mutations for MYH-associated polyposisThomas W Prior, Scott J Bridgeman
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 18, 2006
A feasibility study for the newborn screening of spinal muscular atrophyRobert E Pyatt, Thomas W Prior
The Journal of Molecular Diagnostics : JMD|January 27, 2006
Mutation screening in juvenile polyposis syndromeRobert E Pyatt, Robert Pilarski, Thomas W Prior
The Application of Clinical Genetics|February 3, 2021
Spinal Muscular Atrophy: Mutations, Testing, and Clinical RelevanceMelissa C Keinath, Devin E Prior, Thomas W Prior
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 17, 2004
Technical standards and guidelines for Huntington disease testingNicholas T Potter, Elaine B Spector, Thomas W Prior
Clinical Chemistry|September 25, 2007
Assessment of liquid microbead arrays for the screening of newborns for spinal muscular atrophyRobert E Pyatt, David C Mihal, Thomas W Prior
Molecular Genetics & Genomic Medicine|January 19, 2020
A case report of genetic prion disease with two different PRNP variantsMegan Piazza, Thomas W Prior, Prabhjot S Khalsa, et al.
Birth Defects Research|March 3, 2020
Cytogenetic and molecular diagnostic testing associated with prenatal and postnatal birth defectsStela Z Berisha, Shashi Shetty, Thomas W Prior, et al.
American Journal of Medical Genetics. Part A|September 21, 2004
Homozygous SMN1 deletions in unaffected family members and modification of the phenotype by SMN2Thomas W Prior, Kathryn J Swoboda, H Denman Scott, et al.
Pageof 9

Showing results (11-20 of 82) with videos related to

Sort By:
Pageof 9
The Journal of Molecular Diagnostics : JMD|July 29, 2005
Experience and strategy for the molecular testing of Duchenne muscular dystrophyThomas W Prior, Scott J Bridgeman
Current Protocols in Human Genetics|January 12, 2010
Identifying mutations for MYH-associated polyposisThomas W Prior, Scott J Bridgeman
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 18, 2006
A feasibility study for the newborn screening of spinal muscular atrophyRobert E Pyatt, Thomas W Prior
The Journal of Molecular Diagnostics : JMD|January 27, 2006
Mutation screening in juvenile polyposis syndromeRobert E Pyatt, Robert Pilarski, Thomas W Prior
The Application of Clinical Genetics|February 3, 2021
Spinal Muscular Atrophy: Mutations, Testing, and Clinical RelevanceMelissa C Keinath, Devin E Prior, Thomas W Prior
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 17, 2004
Technical standards and guidelines for Huntington disease testingNicholas T Potter, Elaine B Spector, Thomas W Prior
Clinical Chemistry|September 25, 2007
Assessment of liquid microbead arrays for the screening of newborns for spinal muscular atrophyRobert E Pyatt, David C Mihal, Thomas W Prior
Molecular Genetics & Genomic Medicine|January 19, 2020
A case report of genetic prion disease with two different PRNP variantsMegan Piazza, Thomas W Prior, Prabhjot S Khalsa, et al.
Birth Defects Research|March 3, 2020
Cytogenetic and molecular diagnostic testing associated with prenatal and postnatal birth defectsStela Z Berisha, Shashi Shetty, Thomas W Prior, et al.
American Journal of Medical Genetics. Part A|September 21, 2004
Homozygous SMN1 deletions in unaffected family members and modification of the phenotype by SMN2Thomas W Prior, Kathryn J Swoboda, H Denman Scott, et al.
Pageof 9