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R DuPont

Showing results (81-90 of 135) with videos related to

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American Journal of Medical Genetics. Part A|April 12, 2011
Differential diagnosis of Smith-Magenis syndrome: 1p36 deletion syndromeGustavo H Vieira, Jayson D Rodriguez, Raquel Boy, et al.
Nanomedicine (London, England)|July 28, 2016
The quest for the shortest fragments of A (13-19) and B (12-17) responsible for the aggregation of human insulinMonika Swiontek, Kamil Rozniakowski, Justyna Fraczyk, et al.
Journal of Biomolecular Techniques : JBT|June 6, 2009
ABRF-2002ESRG, a difficult sequence: Analysis of a PVDF-bound known protein with a heterogeneous amino-terminusScott D Buckel, Richard G Cook, J Myron Crawford, et al.
The Journal of Molecular Diagnostics : JMD|February 9, 2023
Clinical Validation and Diagnostic Utility of Optical Genome Mapping in Prenatal Diagnostic TestingNikhil S Sahajpal, Ashis K Mondal, Timothy Fee, et al.
Radiation Research|October 1, 1993
Analysis of somatic cell mutations at the glycophorin A locus in atomic bomb survivors: a comparative study of assay methodsR G Langlois, M Akiyama, Y Kusunoki, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of matrix metalloproteinase 9 (Mmp9) to mouse chromosome 2 bands H1-H2B R DuPont, R Linn, C B Knight, et al.
Hematopathology and Molecular Hematology|January 1, 1997
Translocations of 11q13 in mantle cell lymphoma fail to disrupt the S mu bp-2 geneM L Gulley, Q Zhang, R D Gascoyne, et al.
American Journal of Medical Genetics. Part A|August 12, 2011
Microdeletion at 4q21.3 is associated with intellectual disability, dysmorphic facies, hypotonia, and short statureLynn Dukes-Rimsky, Gregory F Guzauskas, Kenton R Holden, et al.
Molecular Cytogenetics|December 23, 2014
Clinical utility of chromosomal microarray analysis in the diagnosis and management of monosomy 7 mosaicismAlka Chaubey Nee Dwivedi, Michael J Lyons, Kat Kwiatkowski, et al.
Genome Research|March 19, 2025
Optical genome mapping identifies rare structural variants in neural tube defectsNikhil S Sahajpal, Jane Dean, Benjamin Hilton, et al.
Pageof 14

Showing results (81-90 of 135) with videos related to

Sort By:
Pageof 14
American Journal of Medical Genetics. Part A|April 12, 2011
Differential diagnosis of Smith-Magenis syndrome: 1p36 deletion syndromeGustavo H Vieira, Jayson D Rodriguez, Raquel Boy, et al.
Nanomedicine (London, England)|July 28, 2016
The quest for the shortest fragments of A (13-19) and B (12-17) responsible for the aggregation of human insulinMonika Swiontek, Kamil Rozniakowski, Justyna Fraczyk, et al.
Journal of Biomolecular Techniques : JBT|June 6, 2009
ABRF-2002ESRG, a difficult sequence: Analysis of a PVDF-bound known protein with a heterogeneous amino-terminusScott D Buckel, Richard G Cook, J Myron Crawford, et al.
The Journal of Molecular Diagnostics : JMD|February 9, 2023
Clinical Validation and Diagnostic Utility of Optical Genome Mapping in Prenatal Diagnostic TestingNikhil S Sahajpal, Ashis K Mondal, Timothy Fee, et al.
Radiation Research|October 1, 1993
Analysis of somatic cell mutations at the glycophorin A locus in atomic bomb survivors: a comparative study of assay methodsR G Langlois, M Akiyama, Y Kusunoki, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Assignment of matrix metalloproteinase 9 (Mmp9) to mouse chromosome 2 bands H1-H2B R DuPont, R Linn, C B Knight, et al.
Hematopathology and Molecular Hematology|January 1, 1997
Translocations of 11q13 in mantle cell lymphoma fail to disrupt the S mu bp-2 geneM L Gulley, Q Zhang, R D Gascoyne, et al.
American Journal of Medical Genetics. Part A|August 12, 2011
Microdeletion at 4q21.3 is associated with intellectual disability, dysmorphic facies, hypotonia, and short statureLynn Dukes-Rimsky, Gregory F Guzauskas, Kenton R Holden, et al.
Molecular Cytogenetics|December 23, 2014
Clinical utility of chromosomal microarray analysis in the diagnosis and management of monosomy 7 mosaicismAlka Chaubey Nee Dwivedi, Michael J Lyons, Kat Kwiatkowski, et al.
Genome Research|March 19, 2025
Optical genome mapping identifies rare structural variants in neural tube defectsNikhil S Sahajpal, Jane Dean, Benjamin Hilton, et al.
Pageof 14