| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Concordance between Research Sequencing and Clinical Pharmacogenetic Genotyping in the eMERGE-PGx Study
|
Rasmussen-Torvik, Laura J.
|
|
2017
|
19 |
4 |
p. 561-566
6 p.
|
artikel
|
| 2 |
Editorial Board
|
|
|
2017
|
19 |
4 |
p. A1-A2
nvt p.
|
artikel
|
| 3 |
Highly Multiplex Real-Time PCR–Based Screening for Blood-Borne Pathogens on an OpenArray Platform
|
Grigorenko, Elena
|
|
2017
|
19 |
4 |
p. 549-560
12 p.
|
artikel
|
| 4 |
Improving Mutation Screening in Patients with Colorectal Cancer Predisposition Using Next-Generation Sequencing
|
Rey, Jean-Marc
|
|
2017
|
19 |
4 |
p. 589-601
13 p.
|
artikel
|
| 5 |
Minimal Residual Disease Monitoring of Acute Myeloid Leukemia by Massively Multiplex Digital PCR in Patients with NPM1 Mutations
|
Mencia-Trinchant, Nuria
|
|
2017
|
19 |
4 |
p. 537-548
12 p.
|
artikel
|
| 6 |
Molecular Diagnosis of Mosaic Overgrowth Syndromes Using a Custom-Designed Next-Generation Sequencing Panel
|
Chang, Fengqi
|
|
2017
|
19 |
4 |
p. 613-624
12 p.
|
artikel
|
| 7 |
NPM1 for MRD? Droplet Like It's Hot!
|
Wertheim, Gerald B.W.
|
|
2017
|
19 |
4 |
p. 498-501
4 p.
|
artikel
|
| 8 |
Overgrowth Syndromes Caused by Somatic Variants in the Phosphatidylinositol 3-Kinase/AKT/Mammalian Target of Rapamycin Pathway
|
Akgumus, Gozde
|
|
2017
|
19 |
4 |
p. 487-497
11 p.
|
artikel
|
| 9 |
PheoSeq
|
Currás-Freixes, Maria
|
|
2017
|
19 |
4 |
p. 575-588
14 p.
|
artikel
|
| 10 |
Simultaneous Genotyping of α-Thalassemia Deletional and Nondeletional Mutations by Real-Time PCR–Based Multicolor Melting Curve Analysis
|
Huang, Qiuying
|
|
2017
|
19 |
4 |
p. 567-574
8 p.
|
artikel
|
| 11 |
Study of Preanalytic and Analytic Variables for Clinical Next-Generation Sequencing of Circulating Cell-Free Nucleic Acid
|
Mehrotra, Meenakshi
|
|
2017
|
19 |
4 |
p. 514-524
11 p.
|
artikel
|
| 12 |
Table of Contents
|
|
|
2017
|
19 |
4 |
p. A3-A4
nvt p.
|
artikel
|
| 13 |
Technical Validation of a Next-Generation Sequencing Assay for Detecting Clinically Relevant Levels of Breast Cancer–Related Single-Nucleotide Variants and Copy Number Variants Using Simulated Cell-Free DNA
|
Yang, Xin
|
|
2017
|
19 |
4 |
p. 525-536
12 p.
|
artikel
|
| 14 |
Utility of NIST Whole-Genome Reference Materials for the Technical Validation of a Multigene Next-Generation Sequencing Test
|
Shum, Bennett O.V.
|
|
2017
|
19 |
4 |
p. 602-612
11 p.
|
artikel
|
| 15 |
Validation of a Next-Generation Sequencing Pipeline for the Molecular Diagnosis of Multiple Inherited Cancer Predisposing Syndromes
|
Paulo, Paula
|
|
2017
|
19 |
4 |
p. 502-513
12 p.
|
artikel
|
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