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Ben Anderson

Showing results (21-30 of 35) with videos related to

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Molecular Genetics & Genomic Medicine|February 2, 2019
Prenatal cell-free DNA screening for fetal aneuploidy in pregnant women at average or high risk: Results from a large US clinical laboratoryCarrie Guy, Farnoosh Haji-Sheikhi, Charles M Rowland, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|September 11, 2008
Controlled loading of building blocks into temporary self-assembled scaffolds for directed assembly of organic nanostructuresL Todd Banner, Delia C Danila, Katie Sharpe, et al.
The Journal of Molecular Diagnostics : JMD|April 29, 2006
Rapid one-step carrier detection assay of mucolipidosis IV mutations in the Ashkenazi Jewish populationFeras M Hantash, Susan C Olson, Ben Anderson, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|January 24, 2017
Impact of Viral Respiratory Pathogens on Outcomes After Pediatric Cardiac SurgeryKatie Moynihan, Andrew Barlow, Nelson Alphonso, et al.
Prenatal Diagnosis|June 28, 2017
Maternal chromosome Xp deletion identified by prenatal cell-free DNA screeningBernard J Ilagan, Megan D Maxwell, Barbra M Fisher, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 23, 2005
Technical validation of a multiplex platform to detect thirty mutations in eight genetic diseases prevalent in individuals of Ashkenazi Jewish descentCharles M Strom, Richard A Janeczko, Ben Anderson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 17, 2006
CFTR 5T variant has a low penetrance in females that is partially attributable to its haplotypeWeimin Sun, Ben Anderson, Joy Redman, et al.
Human Genetics|December 20, 2005
Novel and recurrent rearrangements in the CFTR gene: clinical and laboratory implications for cystic fibrosis screeningFeras M Hantash, Joy B Redman, Kelsey Starn, et al.
Artificial Organs|January 11, 2016
In Vivo Evaluation of Active and Passive Physiological Control Systems for Rotary Left and Right Ventricular Assist DevicesShaun D Gregory, Michael C Stevens, Jo P Pauls, et al.
Scientific Reports|February 9, 2022
Development and validation of a high throughput SARS-CoV-2 whole genome sequencing workflow in a clinical laboratorySun Hee Rosenthal, Anna Gerasimova, Rolando Ruiz-Vega, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Molecular Genetics & Genomic Medicine|February 2, 2019
Prenatal cell-free DNA screening for fetal aneuploidy in pregnant women at average or high risk: Results from a large US clinical laboratoryCarrie Guy, Farnoosh Haji-Sheikhi, Charles M Rowland, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|September 11, 2008
Controlled loading of building blocks into temporary self-assembled scaffolds for directed assembly of organic nanostructuresL Todd Banner, Delia C Danila, Katie Sharpe, et al.
The Journal of Molecular Diagnostics : JMD|April 29, 2006
Rapid one-step carrier detection assay of mucolipidosis IV mutations in the Ashkenazi Jewish populationFeras M Hantash, Susan C Olson, Ben Anderson, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|January 24, 2017
Impact of Viral Respiratory Pathogens on Outcomes After Pediatric Cardiac SurgeryKatie Moynihan, Andrew Barlow, Nelson Alphonso, et al.
Prenatal Diagnosis|June 28, 2017
Maternal chromosome Xp deletion identified by prenatal cell-free DNA screeningBernard J Ilagan, Megan D Maxwell, Barbra M Fisher, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 23, 2005
Technical validation of a multiplex platform to detect thirty mutations in eight genetic diseases prevalent in individuals of Ashkenazi Jewish descentCharles M Strom, Richard A Janeczko, Ben Anderson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 17, 2006
CFTR 5T variant has a low penetrance in females that is partially attributable to its haplotypeWeimin Sun, Ben Anderson, Joy Redman, et al.
Human Genetics|December 20, 2005
Novel and recurrent rearrangements in the CFTR gene: clinical and laboratory implications for cystic fibrosis screeningFeras M Hantash, Joy B Redman, Kelsey Starn, et al.
Artificial Organs|January 11, 2016
In Vivo Evaluation of Active and Passive Physiological Control Systems for Rotary Left and Right Ventricular Assist DevicesShaun D Gregory, Michael C Stevens, Jo P Pauls, et al.
Scientific Reports|February 9, 2022
Development and validation of a high throughput SARS-CoV-2 whole genome sequencing workflow in a clinical laboratorySun Hee Rosenthal, Anna Gerasimova, Rolando Ruiz-Vega, et al.
Pageof 4