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Matthew J McGinniss

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European Journal of Pediatrics|October 24, 2003
Technology challenges in screening single gene disordersAndreas Braun, Richard Roth, Matthew J McGinniss
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|June 9, 2009
Stratifying risk for celiac disease in a large at-risk United States population by using HLA allelesMichelle M Pietzak, Timothy C Schofield, Matthew J McGinniss, et al.
Evolutionary Bioinformatics Online|May 21, 2009
Multiple property tolerance analysis for the evaluation of missense mutationsTai-Sung Lee, Steven J Potts, Matthew J McGinniss, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|April 20, 2013
Identification of HRAS mutations and absence of GNAQ or GNA11 mutations in deep penetrating neviRyan P Bender, Matthew J McGinniss, Paula Esmay, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 10, 2004
Molecular screening for diseases frequent in Ashkenazi Jews: lessons learned from more than 100,000 tests performed in a commercial laboratoryCharles M Strom, Beryl Crossley, Joy B Redman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 16, 2002
Eight novel mutations in the HEXA geneMatthew J McGinniss, David H Brown, Andrea Fulwiler, et al.
The Journal of Molecular Diagnostics : JMD|August 11, 2007
Characterization of a recurrent novel large duplication in the cystic fibrosis transmembrane conductance regulator geneFeras M Hantash, Joy B Redman, Dana Goos, et al.
The Journal of Molecular Diagnostics : JMD|January 26, 2007
Development of a web-based query tool for quality assurance of clinical molecular genetic test resultsMatthew J McGinniss, Rebecca Chen, Victoria M Pratt, 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.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
European Journal of Pediatrics|October 24, 2003
Technology challenges in screening single gene disordersAndreas Braun, Richard Roth, Matthew J McGinniss
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|June 9, 2009
Stratifying risk for celiac disease in a large at-risk United States population by using HLA allelesMichelle M Pietzak, Timothy C Schofield, Matthew J McGinniss, et al.
Evolutionary Bioinformatics Online|May 21, 2009
Multiple property tolerance analysis for the evaluation of missense mutationsTai-Sung Lee, Steven J Potts, Matthew J McGinniss, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|April 20, 2013
Identification of HRAS mutations and absence of GNAQ or GNA11 mutations in deep penetrating neviRyan P Bender, Matthew J McGinniss, Paula Esmay, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 10, 2004
Molecular screening for diseases frequent in Ashkenazi Jews: lessons learned from more than 100,000 tests performed in a commercial laboratoryCharles M Strom, Beryl Crossley, Joy B Redman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 16, 2002
Eight novel mutations in the HEXA geneMatthew J McGinniss, David H Brown, Andrea Fulwiler, et al.
The Journal of Molecular Diagnostics : JMD|August 11, 2007
Characterization of a recurrent novel large duplication in the cystic fibrosis transmembrane conductance regulator geneFeras M Hantash, Joy B Redman, Dana Goos, et al.
The Journal of Molecular Diagnostics : JMD|January 26, 2007
Development of a web-based query tool for quality assurance of clinical molecular genetic test resultsMatthew J McGinniss, Rebecca Chen, Victoria M Pratt, 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.
Pageof 2