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Tracey Lewis

Showing results (1-10 of 12) with videos related to

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Nursing Management (Harrow, London, England : 1994)|April 17, 2008
How clinical champions can improve qualityTracey Lewis, Carmel Edwards
Ophthalmic Genetics|December 11, 2012
Novel homozygous CYP1B1 deletion in siblings with primary congenital glaucomaKristy Damjanovich, Erin E Baldwin, Tracey Lewis, et al.
BMC Bioinformatics|July 19, 2022
Algorithmic improvements for discovery of germline copy number variants in next-generation sequencing dataBrendan O'Fallon, Jacob Durtschi, Ana Kellogg, et al.
Journal of Obesity|February 17, 2016
A Copy Number Variant on Chromosome 20q13.3 Implicated in Thinness and Severe ObesitySandra J Hasstedt, Yuanpei Xin, Rong Mao, et al.
Obstetrics and Gynecology|June 12, 2003
Pregnancy outcome in recurrent miscarriage patients with skewed X chromosome inactivationAmy E Sullivan, Tracey Lewis, Mary Stephenson, et al.
BMC Medical Genetics|September 23, 2011
Characterization of large genomic deletions in the FBN1 gene using multiplex ligation-dependent probe amplificationLarissa V Furtado, Whitney Wooderchak-Donahue, Alan F Rope, et al.
The Journal of Molecular Diagnostics : JMD|July 14, 2015
Processed Pseudogene Confounding Deletion/Duplication Assays for SMAD4Alison Millson, Tracey Lewis, Tina Pesaran, et al.
Genetic Testing and Molecular Biomarkers|June 22, 2011
Verification of multiplex ligation-dependent probe amplification probes in the absence of positive samplesWhitney Wooderchak-Donahue, Cecily Vaughn, Lan-Szu Chou, et al.
American Journal of Medical Genetics. Part A|May 1, 2012
Candidate locus analysis for PHACE syndromeSheri Mitchell, Dawn H Siegel, Joseph T C Shieh, et al.
The Journal of Molecular Diagnostics : JMD|July 15, 2014
Noncontinuously binding loop-out primers for avoiding problematic DNA sequences in PCR and sanger sequencingKelli Sumner, Jeffrey J Swensen, Melinda Procter, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Nursing Management (Harrow, London, England : 1994)|April 17, 2008
How clinical champions can improve qualityTracey Lewis, Carmel Edwards
Ophthalmic Genetics|December 11, 2012
Novel homozygous CYP1B1 deletion in siblings with primary congenital glaucomaKristy Damjanovich, Erin E Baldwin, Tracey Lewis, et al.
BMC Bioinformatics|July 19, 2022
Algorithmic improvements for discovery of germline copy number variants in next-generation sequencing dataBrendan O'Fallon, Jacob Durtschi, Ana Kellogg, et al.
Journal of Obesity|February 17, 2016
A Copy Number Variant on Chromosome 20q13.3 Implicated in Thinness and Severe ObesitySandra J Hasstedt, Yuanpei Xin, Rong Mao, et al.
Obstetrics and Gynecology|June 12, 2003
Pregnancy outcome in recurrent miscarriage patients with skewed X chromosome inactivationAmy E Sullivan, Tracey Lewis, Mary Stephenson, et al.
BMC Medical Genetics|September 23, 2011
Characterization of large genomic deletions in the FBN1 gene using multiplex ligation-dependent probe amplificationLarissa V Furtado, Whitney Wooderchak-Donahue, Alan F Rope, et al.
The Journal of Molecular Diagnostics : JMD|July 14, 2015
Processed Pseudogene Confounding Deletion/Duplication Assays for SMAD4Alison Millson, Tracey Lewis, Tina Pesaran, et al.
Genetic Testing and Molecular Biomarkers|June 22, 2011
Verification of multiplex ligation-dependent probe amplification probes in the absence of positive samplesWhitney Wooderchak-Donahue, Cecily Vaughn, Lan-Szu Chou, et al.
American Journal of Medical Genetics. Part A|May 1, 2012
Candidate locus analysis for PHACE syndromeSheri Mitchell, Dawn H Siegel, Joseph T C Shieh, et al.
The Journal of Molecular Diagnostics : JMD|July 15, 2014
Noncontinuously binding loop-out primers for avoiding problematic DNA sequences in PCR and sanger sequencingKelli Sumner, Jeffrey J Swensen, Melinda Procter, et al.
Pageof 2