nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
ABL1 gene involvement within a complex three-way translocation (2;9;4) in perineurioma characterized by molecular cytogenetic methods
|
Duff, Deiter J. |
|
2014 |
207 |
6 |
p. 263-267 5 p. |
artikel |
2 |
aCGH+SNP as a Promising Analytical Tool for the Detection of Chromosomal Abnormalities in Acute Leukemia
|
Chen, Chuanfei |
|
2014 |
207 |
6 |
p. 285- 1 p. |
artikel |
3 |
A Mosaic Copy Number Gain of 5p15.3p13.3
|
Valle, Stephanie E. |
|
2014 |
207 |
6 |
p. 286-287 2 p. |
artikel |
4 |
An ider(17)(q10)t(15;17) with spliced long-type PML-RARA fusion transcripts in a case of acute promyelocytic leukemia
|
Hu, Xiaojing |
|
2014 |
207 |
6 |
p. 253-257 5 p. |
artikel |
5 |
A Novel 1p35.1p34.3 Microdeletion in a Baby Boy with Multiple Congenital Anomalies and Developmental Delay
|
Kantarci, Sibel |
|
2014 |
207 |
6 |
p. 290- 1 p. |
artikel |
6 |
Clinical Utility of DNA Arrays in Detecting Chromosomal Aberrations Associated with High-Risk Philadelphia-Like Acute Lymphoblastic Leukemia
|
Raca, Gordana |
|
2014 |
207 |
6 |
p. 284-285 2 p. |
artikel |
7 |
Cover 1
|
|
|
2014 |
207 |
6 |
p. OFC- 1 p. |
artikel |
8 |
Detection of Copy Number Variations in Breast Cancer Samples Using Single-nucleotide Polymorphism-targeted Massively Multiplexed PCR
|
Babiarz, Joshua E. |
|
2014 |
207 |
6 |
p. 287- 1 p. |
artikel |
9 |
Detection of Genomic Imbalances Involved in Common Chromosomal Rearrangements of Acute Leukemia by Cytogenomic SNP Microarray Analysis
|
Yenamandra, A. |
|
2014 |
207 |
6 |
p. 289-290 2 p. |
artikel |
10 |
Editorial Board
|
|
|
2014 |
207 |
6 |
p. IFC- 1 p. |
artikel |
11 |
Effects of TSP-1 -696 C/T polymorphism on bladder cancer susceptibility and clinicopathologic features
|
Gu, Jinbao |
|
2014 |
207 |
6 |
p. 247-252 6 p. |
artikel |
12 |
Extraskeletal myxoid chondrosarcoma with a t(9;16)(q22;p11.2) resulting in a NR4A3-FUS fusion
|
Broehm, Cory J. |
|
2014 |
207 |
6 |
p. 276-280 5 p. |
artikel |
13 |
From chromosomal abnormalities to the identification of target genes in mouse models of breast cancer
|
Fabris, Victoria T. |
|
2014 |
207 |
6 |
p. 233-246 14 p. |
artikel |
14 |
Genome-Wide Microarray Analysis Improves Routine Diagnosis of Hematological Malignancies
|
Shao, Lina |
|
2014 |
207 |
6 |
p. 284- 1 p. |
artikel |
15 |
Integrative Copy Number and Mutational Analysis Improves Glioma Diagnostics
|
Ramkissoon, Shakti H. |
|
2014 |
207 |
6 |
p. 287- 1 p. |
artikel |
16 |
KRAS Amplification in a 73-Year-Old Man with Adenocarcinoma of Lung
|
Chen, Hui |
|
2014 |
207 |
6 |
p. 288- 1 p. |
artikel |
17 |
Microarray Detects Variation in Deletions of IGH (14q32) Gene Region in CLL
|
Utter, Rachel A. |
|
2014 |
207 |
6 |
p. 286- 1 p. |
artikel |
18 |
Molecular Characterization of WNT5B as a Candidate Gene for Developmental Delay Associated with 12p13.13 Microdeletions
|
Omorodion, Jacklyn |
|
2014 |
207 |
6 |
p. 289- 1 p. |
artikel |
19 |
Molecular identification of a TPR-FGFR1 fusion transcript in an adult with myeloproliferative neoplasm, T-lymphoblastic lymphoma, and a t(1;8)(q25;p11.2)
|
Kim, Seon Young |
|
2014 |
207 |
6 |
p. 258-262 5 p. |
artikel |
20 |
Multiple Segmental Chromosomal Aberrations in Low-Risk Neuroblastoma are Associated with Metastatic Relapse
|
Mayfield, Jodi R. |
|
2014 |
207 |
6 |
p. 288- 1 p. |
artikel |
21 |
My Cancer Genome
|
Micheel, Christine M. |
|
2014 |
207 |
6 |
p. 289- 1 p. |
artikel |
22 |
Non-invasive Cell-free Tumor DNA-based Detection of Breast Cancer-related Copy Number Variations
|
Zimmermann, Bernhard G. |
|
2014 |
207 |
6 |
p. 287-288 2 p. |
artikel |
23 |
Old Dog, New Tricks: Novel Application of Whole Genome SNP Microarray for Chimerism Studies in Allogeneic Bone Marrow Transplant Patients
|
Znoyko, Iya Y. |
|
2014 |
207 |
6 |
p. 286- 1 p. |
artikel |
24 |
Rare Complete and Partial Monosomy 7 Mosaicism Detected in a Case with FTT and Borderline Motor Delay, Subsequently Diagnosed with Juvenile MDS: An Exposition of this Case and Other Interesting Mosaic Cancer Case Studies
|
Bickley, Vivienne M. |
|
2014 |
207 |
6 |
p. 286- 1 p. |
artikel |
25 |
Recurrent Genetic Alterations in Hepatitis C-Associated Hepatocellular Carcinoma Detected by Genomic Microarray and Their correlation with Histology and Clinical Outcome
|
Liu, Yajuan |
|
2014 |
207 |
6 |
p. 285- 1 p. |
artikel |
26 |
Secondary Philadelphia chromosome and erythrophagocytosis in a relapsed acute myeloid leukemia after hematopoietic cell transplantation
|
Kelemen, Katalin |
|
2014 |
207 |
6 |
p. 268-271 4 p. |
artikel |
27 |
Table of Contents
|
|
|
2014 |
207 |
6 |
p. A1- 1 p. |
artikel |
28 |
Translocation t(2;7)(p11.2;q21.2): a rare genetic aberration associated with B-cell lymphoproliferative disorders of marginal-zone origin
|
Xochelli, Aliki |
|
2014 |
207 |
6 |
p. 281-283 3 p. |
artikel |
29 |
Validation of Affymetrix Cytoscan HD: Children's Mercy Hospital Experience with Neoplastic Samples
|
Cooley, Linda D. |
|
2014 |
207 |
6 |
p. 284- 1 p. |
artikel |
30 |
What you are missing could matter: a rare, complex BRAF mutation affecting codons 599, 600, and 601 uncovered by next generation sequencing
|
Wilson, Melissa A. |
|
2014 |
207 |
6 |
p. 272-275 4 p. |
artikel |
31 |
Whole Genome Copy Number Analysis of Formalin Fixed Paraffin Embedded Samples Identifies Major Genomic Aberrations in Medulloblastoma
|
Robison, Nathan J. |
|
2014 |
207 |
6 |
p. 290- 1 p. |
artikel |