| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Accurate and Sensitive Analysis of Minimal Residual Disease in Acute Myeloid Leukemia Using Deep Sequencing of Single Nucleotide Variations
|
Delsing Malmberg, Erik
|
|
|
21 |
1 |
p. 149-162
|
artikel
|
| 2 |
A Nanopore Sequencing–Based Assay for Rapid Detection of Gene Fusions
|
Jeck, William R.
|
|
|
21 |
1 |
p. 58-69
|
artikel
|
| 3 |
An Innovative Multiplexed and Flexible Molecular Approach for the Differential Detection of Arboviruses
|
Leon, Fanny
|
|
|
21 |
1 |
p. 81-88
|
artikel
|
| 4 |
An Optimized Workflow to Evaluate Estrogen Receptor Gene Mutations in Small Amounts of Cell-Free DNA
|
Vitale, Silvia R.
|
|
|
21 |
1 |
p. 123-137
|
artikel
|
| 5 |
A Single-Tube, EuroClonality-Inspired, TRG Clonality Multiplex PCR Aids Management of Patients with Enteropathic Diseases, including from Formaldehyde-Fixed, Paraffin-Embedded Tissues
|
Derrieux, Coralie
|
|
|
21 |
1 |
p. 111-122
|
artikel
|
| 6 |
Automated Clinical Exome Reanalysis Reveals Novel Diagnoses
|
Baker, Samuel W.
|
|
|
21 |
1 |
p. 38-48
|
artikel
|
| 7 |
Clinical Evaluation of Massively Parallel RNA Sequencing for Detecting Recurrent Gene Fusions in Hematologic Malignancies
|
Kim, Borahm
|
|
|
21 |
1 |
p. 163-170
|
artikel
|
| 8 |
Diagnostic targETEd seQuencing adjudicaTion (DETEQT)
|
Conrad, Turner A.
|
|
|
21 |
1 |
p. 99-110
|
artikel
|
| 9 |
Editorial Board
|
|
|
|
21 |
1 |
p. A1-A2
|
artikel
|
| 10 |
Evaluation for Genetic Disorders in the Absence of a Clinical Indication for Testing
|
Lu, James T.
|
|
|
21 |
1 |
p. 3-12
|
artikel
|
| 11 |
Expedited Analysis and Reporting of Multiple Mutations that Modify Medical Management of Myeloid Malignancies
|
Kluk, Michael J.
|
|
|
21 |
1 |
p. 13-15
|
artikel
|
| 12 |
insiM
|
Patil, Sushant A.
|
|
|
21 |
1 |
p. 19-26
|
artikel
|
| 13 |
Instructions to Authors
|
|
|
|
21 |
1 |
p. A7-A11
|
artikel
|
| 14 |
Optimized Digital Droplet PCR for BCR-ABL
|
Maier, Jacqueline
|
|
|
21 |
1 |
p. 27-37
|
artikel
|
| 15 |
Rapid Next-Generation Sequencing Method for Prediction of Prostate Cancer Risks
|
Fofanov, Viacheslav Y.
|
|
|
21 |
1 |
p. 49-57
|
artikel
|
| 16 |
Scientific Integrity Policy
|
|
|
|
21 |
1 |
p. A12-A15
|
artikel
|
| 17 |
Screening for Regulatory Variants in 460 kb Encompassing the CFTR Locus in Cystic Fibrosis Patients
|
Kerschner, Jenny L.
|
|
|
21 |
1 |
p. 70-80
|
artikel
|
| 18 |
Table of Contents
|
|
|
|
21 |
1 |
p. A3-A5
|
artikel
|
| 19 |
Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular Aqueduct
|
Lin, Yin-Hung
|
|
|
21 |
1 |
p. 138-148
|
artikel
|
| 20 |
The Next Generation in Detection of Leukemia-Associated Translocations
|
Sabath, Daniel E.
|
|
|
21 |
1 |
p. 16-18
|
artikel
|
| 21 |
Translating Risk of Consumer-Initiated Genetic Testing
|
Zehnbauer, Barbara
|
|
|
21 |
1 |
p. 1-2
|
artikel
|
| 22 |
Ultra-Rapid Reporting of GENomic Targets (URGENTseq)
|
Patel, Keyur P.
|
|
|
21 |
1 |
p. 89-98
|
artikel
|
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