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Peter N Ray

Showing results (1-10 of 62) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|December 21, 2002
Multiplexed fluorescence analysis for mutations causing Tay-Sachs diseaseTracy L Stockley, Peter N Ray
American Journal of Medical Genetics. Part A|June 29, 2010
Paternal isodisomy of chromosome 2 as a cause of long chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiencyBerivan Baskin, Michael Geraghty, Peter N Ray
Neuromuscular Disorders : NMD|December 8, 2010
Duchenne muscular dystrophy caused by a complex rearrangement between intron 43 of the DMD gene and chromosome 4Berivan Baskin, William T Gibson, Peter N Ray
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|August 21, 2002
Gene patents and the standard of careRichard Gold, Timothy A Caulfield, Peter N Ray
American Journal of Medical Genetics|January 25, 2002
Severe and mild phenotypes in Pfeiffer syndrome with splice acceptor mutations in exon IIIc of FGFR2Ahmad S Teebi, Shelley Kennedy, Kathy Chun, et al.
Genetic Testing|January 27, 2007
Strategy for comprehensive molecular testing for Duchenne and Becker muscular dystrophiesTracy L Stockley, Sarah Akber, Natalie Bulgin, et al.
Human Mutation|March 7, 2014
The genome clinic: a multidisciplinary approach to assessing the opportunities and challenges of integrating genomic analysis into clinical careSarah Bowdin, Peter N Ray, Ronald D Cohn, et al.
Pediatric Neurology|October 22, 2013
Eye and brain abnormalities in congenital muscular dystrophies caused by fukutin-related protein gene (FKRP) mutationsMaina Kava, David Chitayat, Susan Blaser, et al.
American Journal of Medical Genetics. Part A|July 29, 2003
Screening of patients with craniosynostosis: molecular strategyKathy Chun, Ahmad S Teebi, Cyrus Azimi, et al.
Clinical Leadership & Management Review : the Journal of CLMA|February 19, 2004
Providing information at the point of care: educational diagnostic reports from a genetic testing service providerLisa M Goos, Irwin Silverman, Leslie Steele, et al.
Pageof 7

Showing results (1-10 of 62) with videos related to

Sort By:
Pageof 7
Methods in Molecular Biology (Clifton, N.J.)|December 21, 2002
Multiplexed fluorescence analysis for mutations causing Tay-Sachs diseaseTracy L Stockley, Peter N Ray
American Journal of Medical Genetics. Part A|June 29, 2010
Paternal isodisomy of chromosome 2 as a cause of long chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiencyBerivan Baskin, Michael Geraghty, Peter N Ray
Neuromuscular Disorders : NMD|December 8, 2010
Duchenne muscular dystrophy caused by a complex rearrangement between intron 43 of the DMD gene and chromosome 4Berivan Baskin, William T Gibson, Peter N Ray
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|August 21, 2002
Gene patents and the standard of careRichard Gold, Timothy A Caulfield, Peter N Ray
American Journal of Medical Genetics|January 25, 2002
Severe and mild phenotypes in Pfeiffer syndrome with splice acceptor mutations in exon IIIc of FGFR2Ahmad S Teebi, Shelley Kennedy, Kathy Chun, et al.
Genetic Testing|January 27, 2007
Strategy for comprehensive molecular testing for Duchenne and Becker muscular dystrophiesTracy L Stockley, Sarah Akber, Natalie Bulgin, et al.
Human Mutation|March 7, 2014
The genome clinic: a multidisciplinary approach to assessing the opportunities and challenges of integrating genomic analysis into clinical careSarah Bowdin, Peter N Ray, Ronald D Cohn, et al.
Pediatric Neurology|October 22, 2013
Eye and brain abnormalities in congenital muscular dystrophies caused by fukutin-related protein gene (FKRP) mutationsMaina Kava, David Chitayat, Susan Blaser, et al.
American Journal of Medical Genetics. Part A|July 29, 2003
Screening of patients with craniosynostosis: molecular strategyKathy Chun, Ahmad S Teebi, Cyrus Azimi, et al.
Clinical Leadership & Management Review : the Journal of CLMA|February 19, 2004
Providing information at the point of care: educational diagnostic reports from a genetic testing service providerLisa M Goos, Irwin Silverman, Leslie Steele, et al.
Pageof 7