Andrew G Hadd - JoVE Visualize

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The Journal of Organic Chemistry|April 19, 1996

Kinetics and Mechanism of the Nucleophilic Substitution Reaction of Imidazole with Bis(2,4,6-trichlorophenyl) Oxalate and Bis(2,4-dinitrophenyl) OxalateAndrew G. Hadd, John W. Birks

Molecular Biotechnology|February 8, 2012

A dual-mode single-molecule fluorescence assay for the detection of expanded CGG repeats in Fragile X syndromeBrian Cannon, Cynthia Pan, Liangjing Chen, et al.

BMC Medical Genetics|August 5, 2006

Polymorphisms in the glucocerebrosidase gene and pseudogene urge caution in clinical analysis of Gaucher disease allele c.1448T>C (L444P)Justin T Brown, Cora Lahey, Walairat Laosinchai-Wolf, et al.

Frontiers in Genetics|August 15, 2014

The role of AGG interruptions in fragile X repeat expansions: a twenty-year perspectiveGary J Latham, Justine Coppinger, Andrew G Hadd, et al.

Journal of Visualized Experiments : Jove|May 12, 2016

Integration of Wet and Dry Bench Processes Optimizes Targeted Next-generation Sequencing of Low-quality and Low-quantity Tumor BiopsiesJeffrey Houghton, Andrew G Hadd, Robert Zeigler, et al.

Expert Review of Molecular Diagnostics|June 7, 2005

Adoption of array technologies into the clinical laboratoryAndrew G Hadd, Justin T Brown, Bernard F Andruss, et al.

Menopause (New York, N.Y.)|January 16, 2014

Intermediate CGG repeat length at the FMR1 locus is not associated with hormonal indicators of ovarian ageJennie K Kline, Ann M Kinney, Bruce Levin, et al.

Neurology. Genetics|April 12, 2016

X-inactivation in the clinical phenotype of fragile X premutation carrier sistersDeborah A Hall, Erin E Robertson-Dick, Joan A O'Keefe, et al.

Clinical Epigenetics|December 17, 2016

A methylation PCR method determines <i>FMR1</i> activation ratios and differentiates premutation allele mosaicism in carrier siblingsAndrew G Hadd, Stela Filipovic-Sadic, Lili Zhou, et al.

The Journal of Molecular Diagnostics : JMD|October 28, 2004

Microsphere bead arrays and sequence validation of 5/7/9T genotypes for multiplex screening of cystic fibrosis polymorphismsAndrew G Hadd, Walairat Laosinchai-Wolf, Chris R Novak, et al.

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Showing results (1-10 of 19) with videos related to

Sort By:

Pageof 2

The Journal of Organic Chemistry|April 19, 1996

Kinetics and Mechanism of the Nucleophilic Substitution Reaction of Imidazole with Bis(2,4,6-trichlorophenyl) Oxalate and Bis(2,4-dinitrophenyl) OxalateAndrew G. Hadd, John W. Birks

Molecular Biotechnology|February 8, 2012

A dual-mode single-molecule fluorescence assay for the detection of expanded CGG repeats in Fragile X syndromeBrian Cannon, Cynthia Pan, Liangjing Chen, et al.

BMC Medical Genetics|August 5, 2006

Polymorphisms in the glucocerebrosidase gene and pseudogene urge caution in clinical analysis of Gaucher disease allele c.1448T>C (L444P)Justin T Brown, Cora Lahey, Walairat Laosinchai-Wolf, et al.

Frontiers in Genetics|August 15, 2014

The role of AGG interruptions in fragile X repeat expansions: a twenty-year perspectiveGary J Latham, Justine Coppinger, Andrew G Hadd, et al.

Journal of Visualized Experiments : Jove|May 12, 2016

Integration of Wet and Dry Bench Processes Optimizes Targeted Next-generation Sequencing of Low-quality and Low-quantity Tumor BiopsiesJeffrey Houghton, Andrew G Hadd, Robert Zeigler, et al.

Expert Review of Molecular Diagnostics|June 7, 2005

Adoption of array technologies into the clinical laboratoryAndrew G Hadd, Justin T Brown, Bernard F Andruss, et al.

Menopause (New York, N.Y.)|January 16, 2014

Intermediate CGG repeat length at the FMR1 locus is not associated with hormonal indicators of ovarian ageJennie K Kline, Ann M Kinney, Bruce Levin, et al.

Neurology. Genetics|April 12, 2016

X-inactivation in the clinical phenotype of fragile X premutation carrier sistersDeborah A Hall, Erin E Robertson-Dick, Joan A O'Keefe, et al.

Clinical Epigenetics|December 17, 2016

A methylation PCR method determines <i>FMR1</i> activation ratios and differentiates premutation allele mosaicism in carrier siblingsAndrew G Hadd, Stela Filipovic-Sadic, Lili Zhou, et al.

The Journal of Molecular Diagnostics : JMD|October 28, 2004

Microsphere bead arrays and sequence validation of 5/7/9T genotypes for multiplex screening of cystic fibrosis polymorphismsAndrew G Hadd, Walairat Laosinchai-Wolf, Chris R Novak, et al.

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