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                             16 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A Highly Sensitive and Robust Method for Hepatitis B Virus Covalently Closed Circular DNA Detection in Single Cells and Serum Huang, Jing-Tao
2018
20 3 p. 334-343
artikel
2 An In-Depth Evaluation of the Validity and Logistics Surrounding the Testing of AR-V7 mRNA Expression in Circulating Tumor Cells Sieuwerts, Anieta M.
2018
20 3 p. 316-325
artikel
3 Chimerism Analysis in the Pediatric Setting Kricke, Susanne
2018
20 3 p. 381-388
artikel
4 Clustered Regularly Interspaced Short Palindromic Repeat (CRISPR)/CRISPR-Associated Endonuclease Cas9–Mediated Homology-Independent Integration for Generating Quality Control Materials for Clinical Molecular Genetic Testing Lin, Guigao
2018
20 3 p. 373-380
artikel
5 Deciphering Elevated Microsatellite Alterations at Selected Tetra/Pentanucleotide Repeats, Microsatellite Instability, and Loss of Heterozygosity in Colorectal Cancers Wang, Yang
2018
20 3 p. 366-372
artikel
6 Editorial Board 2018
20 3 p. A1-A2
artikel
7 Evaluation of Two Commercial Real-Time PCR Kits for Aspergillus DNA Detection in Bronchoalveolar Lavage Fluid in Patients with Invasive Pulmonary Aspergillosis Denis, Julie
2018
20 3 p. 298-306
artikel
8 Hepatitis B Virus Covalently Closed Circular DNA–Selective Droplet Digital PCR Shen, Fan
2018
20 3 p. 277-278
artikel
9 Optimal Reference Gene Selection for Expression Studies in Human Reticulocytes Aggarwal, Anu
2018
20 3 p. 326-333
artikel
10 Rapid, Loop-Mediated Isothermal Amplification Detection of Celiac Disease Risk Alleles Erlichster, Michael
2018
20 3 p. 307-315
artikel
11 Recommendations for Clinical CYP2C19 Genotyping Allele Selection Pratt, Victoria M.
2018
20 3 p. 269-276
artikel
12 Reference Size Matching, Whole-Genome Amplification, and Fluorescent Labeling as a Method for Chromosomal Microarray Analysis of Clinically Actionable Copy Number Alterations in Formalin-Fixed, Paraffin-Embedded Tumor Tissue Gunn, Shelly R.
2018
20 3 p. 279-288
artikel
13 Spinocerebellar Ataxia Tethering PCR Cagnoli, Claudia
2018
20 3 p. 289-297
artikel
14 Table of Contents 2018
20 3 p. A3-A4
artikel
15 Targeted Next-Generation Sequencing Is a Sensitive Tool for Differential Diagnosis of Myelodysplastic Syndromes in Bone Marrow Trephines Bräuninger, Andreas
2018
20 3 p. 344-354
artikel
16 Validation of a Customized Bioinformatics Pipeline for a Clinical Next-Generation Sequencing Test Targeting Solid Tumor–Associated Variants Schneider, Thomas
2018
20 3 p. 355-365
artikel
                             16 gevonden resultaten
 
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