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Kelli Sumner

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

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The Journal of Hand Surgery, European Volume|April 18, 2018
An investigation of PIK3CA mutations in isolated macrodactylyJingheng Wu, Wei Tian, Guanglei Tian, et al.
G3 (Bethesda, Md.)|March 3, 2012
The SPRED1 Variants Repository for Legius SyndromeKelli Sumner, David K Crockett, Talia Muram, et al.
Human Mutation|June 25, 2010
The Alport syndrome COL4A5 variant databaseDavid K Crockett, Genevieve Pont-Kingdon, Frederick Gedge, et al.
Clinical Chemistry|April 12, 2008
Design and application of noncontinuously binding probes used for haplotyping and genotypingGenevieve Pont-Kingdon, Rebecca L Margraf, Kelli Sumner, et al.
BMC Nephrology|November 19, 2009
Molecular testing for adult type Alport syndromeGenevieve Pont-Kingdon, Kelli Sumner, Friederike Gedge, et al.
Biotechniques|March 22, 2007
Multiplex genotyping by melting analysis of loci-spanning probes: beta-globin as an exampleGenevieve Pont-Kingdon, Lan-Szu Chou, Kristy Damjanovich, et al.
Cardiology in the Young|July 16, 2015
Infantile pulmonary capillary haemangiomatosis: a lethal form of pulmonary hypertensionEiméar McGovern, Paul McNally, Maureen O'Sullivan, et al.
Genetic Testing and Molecular Biomarkers|January 25, 2011
Implementation of a cost-effective unlabeled probe high-resolution melt assay for genotyping of Factor V LeidenAnnika M Svensson, Lan-Szu Chou, Cindy Meadows, 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.
Genetic Testing and Molecular Biomarkers|February 28, 2012
Validation of an unlabeled probe melting analysis assay combined with high-throughput extractions for genotyping of the most common variants in HFE-associated hereditary hemochromatosis, C282Y, H63D, and S65CKelli Sumner, Lindsey Hubley, Genevieve Pont-Kingdon, et al.
Pageof 2

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

Sort By:
Pageof 2
The Journal of Hand Surgery, European Volume|April 18, 2018
An investigation of PIK3CA mutations in isolated macrodactylyJingheng Wu, Wei Tian, Guanglei Tian, et al.
G3 (Bethesda, Md.)|March 3, 2012
The SPRED1 Variants Repository for Legius SyndromeKelli Sumner, David K Crockett, Talia Muram, et al.
Human Mutation|June 25, 2010
The Alport syndrome COL4A5 variant databaseDavid K Crockett, Genevieve Pont-Kingdon, Frederick Gedge, et al.
Clinical Chemistry|April 12, 2008
Design and application of noncontinuously binding probes used for haplotyping and genotypingGenevieve Pont-Kingdon, Rebecca L Margraf, Kelli Sumner, et al.
BMC Nephrology|November 19, 2009
Molecular testing for adult type Alport syndromeGenevieve Pont-Kingdon, Kelli Sumner, Friederike Gedge, et al.
Biotechniques|March 22, 2007
Multiplex genotyping by melting analysis of loci-spanning probes: beta-globin as an exampleGenevieve Pont-Kingdon, Lan-Szu Chou, Kristy Damjanovich, et al.
Cardiology in the Young|July 16, 2015
Infantile pulmonary capillary haemangiomatosis: a lethal form of pulmonary hypertensionEiméar McGovern, Paul McNally, Maureen O'Sullivan, et al.
Genetic Testing and Molecular Biomarkers|January 25, 2011
Implementation of a cost-effective unlabeled probe high-resolution melt assay for genotyping of Factor V LeidenAnnika M Svensson, Lan-Szu Chou, Cindy Meadows, 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.
Genetic Testing and Molecular Biomarkers|February 28, 2012
Validation of an unlabeled probe melting analysis assay combined with high-throughput extractions for genotyping of the most common variants in HFE-associated hereditary hemochromatosis, C282Y, H63D, and S65CKelli Sumner, Lindsey Hubley, Genevieve Pont-Kingdon, et al.
Pageof 2