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J Latham

Showing results (161-170 of 200) with videos related to

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The Journal of Molecular Diagnostics : JMD|December 24, 2019
Validation of Fragile X Screening in the Newborn Population Using a Fit-for-Purpose FMR1 PCR Assay SystemStacey Lee, Jennifer L Taylor, Charles Redmond, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 12, 2014
Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriersSarah L Nolin, Anne Glicksman, Nicole Ersalesi, et al.
BMC Medical Genomics|November 15, 2014
Evaluation of an integrated clinical workflow for targeted next-generation sequencing of low-quality tumor DNA using a 51-gene enrichment panelAshish Choudhary, Elizabeth Mambo, Tiffany Sanford, et al.
Journal of Patient Experience|January 22, 2025
The Diagnostic Journey of Dysautonomia Patients: Insights from a Patient-Reported Outcome StudyJohn A O'Dell, Ash Walker, Andrew J Latham, et al.
The Journal of Molecular Diagnostics : JMD|November 2, 2013
A novel methylation PCR that offers standardized determination of FMR1 methylation and CGG repeat length without southern blot analysisMarina Grasso, Elles M J Boon, Stela Filipovic-Sadic, et al.
The Journal of Molecular Diagnostics : JMD|July 10, 2010
An information-rich CGG repeat primed PCR that detects the full range of fragile X expanded alleles and minimizes the need for southern blot analysisLiangjing Chen, Andrew Hadd, Sachin Sah, et al.
Anesthesia and Analgesia|September 19, 2017
Consensus Statement by the Congenital Cardiac Anesthesia Society: Milestones for the Pediatric Cardiac Anesthesia FellowshipViviane G Nasr, Nina A Guzzetta, Wanda C Miller-Hance, et al.
Clinical Chemistry|January 9, 2010
A novel FMR1 PCR method for the routine detection of low abundance expanded alleles and full mutations in fragile X syndromeStela Filipovic-Sadic, Sachin Sah, Liangjing Chen, et al.
Archives of Biochemistry and Biophysics|July 15, 1996
Effects of freezing, thawing, and storing human liver microsomes on cytochrome P450 activityR E Pearce, C J McIntyre, A Madan, et al.
American Journal of Medical Genetics. Part A|May 4, 2019
Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation allelesSarah L Nolin, Anne Glicksman, Nicole Tortora, et al.
Pageof 20

Showing results (161-170 of 200) with videos related to

Sort By:
Pageof 20
The Journal of Molecular Diagnostics : JMD|December 24, 2019
Validation of Fragile X Screening in the Newborn Population Using a Fit-for-Purpose FMR1 PCR Assay SystemStacey Lee, Jennifer L Taylor, Charles Redmond, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 12, 2014
Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriersSarah L Nolin, Anne Glicksman, Nicole Ersalesi, et al.
BMC Medical Genomics|November 15, 2014
Evaluation of an integrated clinical workflow for targeted next-generation sequencing of low-quality tumor DNA using a 51-gene enrichment panelAshish Choudhary, Elizabeth Mambo, Tiffany Sanford, et al.
Journal of Patient Experience|January 22, 2025
The Diagnostic Journey of Dysautonomia Patients: Insights from a Patient-Reported Outcome StudyJohn A O'Dell, Ash Walker, Andrew J Latham, et al.
The Journal of Molecular Diagnostics : JMD|November 2, 2013
A novel methylation PCR that offers standardized determination of FMR1 methylation and CGG repeat length without southern blot analysisMarina Grasso, Elles M J Boon, Stela Filipovic-Sadic, et al.
The Journal of Molecular Diagnostics : JMD|July 10, 2010
An information-rich CGG repeat primed PCR that detects the full range of fragile X expanded alleles and minimizes the need for southern blot analysisLiangjing Chen, Andrew Hadd, Sachin Sah, et al.
Anesthesia and Analgesia|September 19, 2017
Consensus Statement by the Congenital Cardiac Anesthesia Society: Milestones for the Pediatric Cardiac Anesthesia FellowshipViviane G Nasr, Nina A Guzzetta, Wanda C Miller-Hance, et al.
Clinical Chemistry|January 9, 2010
A novel FMR1 PCR method for the routine detection of low abundance expanded alleles and full mutations in fragile X syndromeStela Filipovic-Sadic, Sachin Sah, Liangjing Chen, et al.
Archives of Biochemistry and Biophysics|July 15, 1996
Effects of freezing, thawing, and storing human liver microsomes on cytochrome P450 activityR E Pearce, C J McIntyre, A Madan, et al.
American Journal of Medical Genetics. Part A|May 4, 2019
Expansions and contractions of the FMR1 CGG repeat in 5,508 transmissions of normal, intermediate, and premutation allelesSarah L Nolin, Anne Glicksman, Nicole Tortora, et al.
Pageof 20