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Molecular Genetics & Genomic Medicine|April 12, 2016
Next generation sequencing-based copy number analysis reveals low prevalence of deletions and duplications in 46 genes associated with genetic cardiomyopathiesOzge Ceyhan-Birsoy, Trevor J Pugh, Mark J Bowser, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 2, 1999
c-erbB-2/EGFR as dominant heterodimerization partners determine a motogenic phenotype in human breast cancer cellsB H Brandt, A Roetger, T Dittmar, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 13, 2015
Improving hearing loss gene testing: a systematic review of gene evidence toward more efficient next-generation sequencing-based diagnostic testing and interpretationAhmad N Abou Tayoun, Saeed H Al Turki, Andrea M Oza, et al.
Genetic Testing|March 31, 2007
A novel, single nucleotide polymorphism-based assay to detect 22q11 deletionsBirgit H Funke, Alison C Brown, Marco F Ramoni, et al.
The Journal of Molecular Diagnostics : JMD|August 27, 2014
Comprehensive diagnostic testing for stereocilin: an approach for analyzing medically important genes with high homologyDiana Mandelker, Sami S Amr, Trevor Pugh, et al.
Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|June 1, 1983
[Candidate selected method for the enzymatic determination of total cholesterol in serum]R Kattermann, I R Kupke, K Borner, et al.
The Journal of Molecular Diagnostics : JMD|September 25, 2010
Evaluation of second-generation sequencing of 19 dilated cardiomyopathy genes for clinical applicationsSivakumar Gowrisankar, Jordan P Lerner-Ellis, Stephanie Cox, et al.
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