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Genetic Testing and Molecular Biomarkers|October 21, 2015
The Frequency of c.550delA Mutation of the CANP3 Gene in the Polish LGMD2A PopulationMałgorzata Dorobek, Barbara Ryniewicz, Dagmara Kabzińska, et al.Genetic Testing and Molecular Biomarkers|October 28, 2015
Development and Validation of a New Molecular Diagnostic Assay for Detection of Myotonic Dystrophy Type 2Rea Valaperta, Fortunata Lombardi, Rosanna Cardani, et al.Genetic Testing and Molecular Biomarkers|October 28, 2015
The Frequency of Methylation Abnormalities Among Estonian Patients Selected by Clinical Diagnostic Scoring Systems for Silver-Russell Syndrome and Beckwith-Wiedemann SyndromeMari-Anne Vals, Maria Yakoreva, Tiina Kahre, et al.Genetic Testing and Molecular Biomarkers|November 7, 2015
Chromogenic Assay for Lung Cancer-Related EGFR Exon 19 Hotspot Deletion MutationsAndy K ZhangGenetic Testing and Molecular Biomarkers|May 27, 2016
Role of SEP15 Gene Polymorphisms in the Time of Progression to AIDSJéssica Louise Benelli, Rúbia Marília de Medeiros, Maria Cristina Cotta Matte, et al.Genetic Testing and Molecular Biomarkers|March 9, 2016
Association Between the Transforming Growth Factor Beta 1 Gene Polymorphisms and Turkish Patients with Nonsyndromic Cleft Lip With/Without Cleft PalateDeniz Aslar Oner, Hakki TastanGenetic Testing and Molecular Biomarkers|February 25, 2016
MiRNA-Related Polymorphisms in miR-146a and TCF21 Are Associated with Increased Susceptibility to Coronary Artery Disease in an Iranian PopulationMilad Bastami, Sayyed Mohamad Hossein Ghaderian, Mir Davood Omrani, et al.Genetic Testing and Molecular Biomarkers|July 19, 2013
Informing public health policy through deliberative public engagement: perceived impact on participants and citizen-government relationsCaron Molster, Ayla Potts, Beverley McNamara, et al.Genetic Testing and Molecular Biomarkers|June 14, 2012
Complete FXN deletion in a patient with Friedreich's ataxiaAns M W van den Ouweland, Rick van Minkelen, Galhana M Bolman, et al.Genetic Testing and Molecular Biomarkers|January 1, 2015
The association of MDM2 c.346G>A genetic variant with the risk of osteosarcoma in ChineseZhaohui Hu, Ningning Li, Xiangtao Xie, et al.Pageof 193