| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Case of Acute Myeloid Leukemia with Novel Dicentric and Ring of Chromosome 22
|
Cong, Hoang Tran
|
|
2016
|
212-213 |
5 |
p. 243-
1 p.
|
artikel
|
| 2 |
A Case of “Triple-Hit” Lymphoma Diagnosed by Integrated Cytogenetic Approaches: FISH, Karyotyping and Microarray
|
Xu, Dongbin
|
|
2016
|
212-213 |
5 |
p. 241-
1 p.
|
artikel
|
| 3 |
A case with a cytogenetically cryptic variant of the inv(16)(p13q22)/t(16;16)(p13;q22)
|
Van Obbergh, Florence
|
|
2014
|
212-213 |
5 |
p. 231-232
2 p.
|
artikel
|
| 4 |
Acute panmyelosis with myelofibrosis with EVI1 amplification
|
Grygalewicz, Beata
|
|
2012
|
212-213 |
5 |
p. 255-260
6 p.
|
artikel
|
| 5 |
An insertion/deletion polymorphism in the 3′ untranslated region of type I collagen a2 (COL1A2) is associated with susceptibility for hepatocellular carcinoma in a Chinese population
|
Zhu, Zhansheng
|
|
2011
|
212-213 |
5 |
p. 265-269
5 p.
|
artikel
|
| 6 |
An Isogenic Trisomic–Disomic Model System Using Cells from People with Mosaic Down Syndrome Unmasks Trisomy 21 Associated Increases in Age-Related Chromosomal Instability, Senescence Associated Distension of Satellites, and Telomere Shortening
|
Rafferty, Kelly
|
|
2016
|
212-213 |
5 |
p. 238-
1 p.
|
artikel
|
| 7 |
A Novel BCL2 Gene Rearrangement, t(5;18)(q31;q21), in Follicular Lymphoma
|
Kantarci, Sibel
|
|
2013
|
212-213 |
5 |
p. 212-
1 p.
|
artikel
|
| 8 |
A Novel Three-Way Rearrangement Involving ETV6 (12p13) and ABL1 (9q34) in Acute Myeloid Leukemia
|
Siangchin, Ken
|
|
2016
|
212-213 |
5 |
p. 242-
1 p.
|
artikel
|
| 9 |
An Unbalanced Translocation Between Chromosomes 1 and 5 in T-Cell Acute Lymphoblastic Leukemia: A Case Report
|
Cheng, Dongsheng
|
|
2016
|
212-213 |
5 |
p. 242-243
2 p.
|
artikel
|
| 10 |
A Rare Case of Russell-Silver and 1p36 Deletion Syndromes
|
Blackwell, Donna
|
|
2016
|
212-213 |
5 |
p. 237-
1 p.
|
artikel
|
| 11 |
A role for epigenetics in the formation of chromosome translocations in acute leukemia
|
Gill Super, Heidi J.
|
|
2015
|
212-213 |
5 |
p. 230-236
7 p.
|
artikel
|
| 12 |
Assessing Copy Number Variants Involving ACMGG Secondary Finding Genes Identified by Routine Chromosomal SNP Array in a Clinical Pediatric Population
|
Fan, Jinbo
|
|
2016
|
212-213 |
5 |
p. 230-
1 p.
|
artikel
|
| 13 |
Associations of THBS2 and THBS4 polymorphisms to gastric cancer in a Southeast Chinese population
|
Lin, Xiandong
|
|
2016
|
212-213 |
5 |
p. 215-222
8 p.
|
artikel
|
| 14 |
A three-way translocation of MLL, MLLT11, and the novel reciprocal partner gene MYO18A in a child with acute myeloid leukemia
|
Ussowicz, Marek
|
|
2012
|
212-213 |
5 |
p. 261-265
5 p.
|
artikel
|
| 15 |
A Variant of inv(3)(q21q26.2) or t(3;3)(q21;q26.2) (MECOM) Rearrangement in AML
|
Mueller, Rosemary
|
|
2016
|
212-213 |
5 |
p. 244-
1 p.
|
artikel
|
| 16 |
BCR–JAK2 fusion in a myeloproliferative neoplasm with associated eosinophilia
|
He, Rong
|
|
2016
|
212-213 |
5 |
p. 223-228
6 p.
|
artikel
|
| 17 |
Bi-allelic Amplification of ATM Gene in Blastoid Variant of Mantle Cell Lymphoma: A Novel Mechanism of Inactivation Due to Chromothripsis?
|
Mendiola, Christina
|
|
2016
|
212-213 |
5 |
p. 244-
1 p.
|
artikel
|
| 18 |
Case Report of a Complex Supernumerary Chromosome That Represents Constitutional Chromoanagenesis
|
Haddadin, Mary
|
|
2016
|
212-213 |
5 |
p. 249-
1 p.
|
artikel
|
| 19 |
Case Report: Unbalanced Translocation Causing Terminal Deletion of 11q25 to 11qter and Terminal Duplication of 12q24 to 12qter in Addition to 16q24.2 Deletion
|
Abdulwahed, Omaiyah Al
|
|
2016
|
212-213 |
5 |
p. 248-
1 p.
|
artikel
|
| 20 |
Characterization of a Complex Derivative Chromosome 18
|
Penton, Andrea
|
|
2016
|
212-213 |
5 |
p. 247-248
2 p.
|
artikel
|
| 21 |
Characterization of Chromosome Translocation Breakpoints in Leukemia Using Whole Genome Mate-Pair Sequencing
|
Qi, Zhongxia(Joe)
|
|
2016
|
212-213 |
5 |
p. 236-
1 p.
|
artikel
|
| 22 |
Chromosomal Microarray as a First Tier Test Following Diagnostic Prenatal Procedure. The Toronto Mount Sinai Hospital Experience
|
Kolomietz, Elena
|
|
2016
|
212-213 |
5 |
p. 229-230
2 p.
|
artikel
|
| 23 |
Chromosomal translocations involving the IGH@ locus in B-cell precursor acute lymphoblastic leukemia: 29 new cases and a review of the literature
|
Chapiro, Elise
|
|
2013
|
212-213 |
5 |
p. 162-173
12 p.
|
artikel
|
| 24 |
Clinical Impact of Genomic Duplications: A Discussion of Reporting Practices
|
Marcou, Cherisse A.
|
|
2016
|
212-213 |
5 |
p. 230-231
2 p.
|
artikel
|
| 25 |
Clinical Utility of SNP Microarrays in Adult Brain Tumors: Molecular Insight into Tumor Heterogeneity and Progression
|
Znoyko, Iya
|
|
2013
|
212-213 |
5 |
p. 215-
1 p.
|
artikel
|
| 26 |
Clinical Utility of the Detection of Genomic Aberrations in Formalin-Fixed Paraffin-Embedded Myeloid Sarcoma Samples
|
Sukhanova, Madina
|
|
2013
|
212-213 |
5 |
p. 214-215
2 p.
|
artikel
|
| 27 |
Clinical Validation of a Simple FISH Assay That Uses 1 µl of Probe
|
Stanchfield, James
|
|
2016
|
212-213 |
5 |
p. 249-
1 p.
|
artikel
|
| 28 |
CNVs Provide the Clue for a Cryptic t(5;11) in Acute Myeloid Leukemia
|
Chia, Nicole L.
|
|
2013
|
212-213 |
5 |
p. 211-
1 p.
|
artikel
|
| 29 |
Complex Cases: Putting It All Together Using the Tools in Your Toolbox (Microarray, FISH and Chromosome Analysis)
|
Smolarek, Teresa A.
|
|
2016
|
212-213 |
5 |
p. 230-
1 p.
|
artikel
|
| 30 |
Comprehensive BRCA1 and BRCA2 mutational profile in Lithuania
|
Janavičius, Ramūnas
|
|
2014
|
212-213 |
5 |
p. 195-205
11 p.
|
artikel
|
| 31 |
Correlating Copy Number Alterations in Dedifferentiated Liposarcoma With Tumor Behavior and Patient Outcome
|
Liu, Yajuan
|
|
2016
|
212-213 |
5 |
p. 232-
1 p.
|
artikel
|
| 32 |
Correlating Hepatoblastoma Outcome With Karyotype and Microarray Data—A Pilot Study
|
Cooley, Linda
|
|
2016
|
212-213 |
5 |
p. 242-
1 p.
|
artikel
|
| 33 |
Correlation of polypoid colorectal adenocarcinoma with pre-existing adenomatous polyps and KRAS mutation
|
Chen, Hui
|
|
2011
|
212-213 |
5 |
p. 245-251
7 p.
|
artikel
|
| 34 |
Cover 1
|
|
|
2014
|
212-213 |
5 |
p. OFC-
1 p.
|
artikel
|
| 35 |
Cover 1
|
|
|
2015
|
212-213 |
5 |
p. OFC-
1 p.
|
artikel
|
| 36 |
Cover 1
|
|
|
2013
|
212-213 |
5 |
p. OFC-
1 p.
|
artikel
|
| 37 |
Cover 1
|
|
|
2012
|
212-213 |
5 |
p. OFC-
1 p.
|
artikel
|
| 38 |
Cover 1
|
|
|
2011
|
212-213 |
5 |
p. OFC-
1 p.
|
artikel
|
| 39 |
Cover_spine
|
|
|
2016
|
212-213 |
5 |
p. CO1-
1 p.
|
artikel
|
| 40 |
CTLA-4 gene polymorphism at position +49 A>G in exon 1: a risk factor for cervical cancer in Indian women
|
Gokhale, Priyanka
|
|
2013
|
212-213 |
5 |
p. 154-161
8 p.
|
artikel
|
| 41 |
Current state of pediatric sarcoma biology and opportunities for future discovery: A report from the sarcoma translational research workshop
|
Hingorani, Pooja
|
|
2016
|
212-213 |
5 |
p. 182-194
13 p.
|
artikel
|
| 42 |
Cytogenetics of Infant/Congenital Leukemia: Mayo Clinic Experience From 2005–2015
|
Cao, Yang
|
|
2016
|
212-213 |
5 |
p. 232-
1 p.
|
artikel
|
| 43 |
Cytogenetic Studies Supporting the Development of New Immunotherapy for B-cell Acute Lymphoblastic Leukemia
|
Aikawa, Vania
|
|
2016
|
212-213 |
5 |
p. 233-
1 p.
|
artikel
|
| 44 |
Development of a Chromosomal Microarray Test for the Detection of Abnormalities in Formalin-Fixed Paraffin-Embedded Products of Conception Specimens
|
Gliem, Troy J.
|
|
2016
|
212-213 |
5 |
p. 240-241
2 p.
|
artikel
|
| 45 |
Differences in the cytogenetic alteration profiles of diffuse large B-cell lymphoma among Chinese and American patients
|
Chen, Yan
|
|
2013
|
212-213 |
5 |
p. 183-190
8 p.
|
artikel
|
| 46 |
Direct FISH, Cultured Chromosome Analysis, and Direct SNP Microarray Analysis in Identifying Ring Chromosomes on Prenatal Analysis: A Case of 45,X/46,X,r(X)
|
Risheg, Hiba
|
|
2016
|
212-213 |
5 |
p. 229-
1 p.
|
artikel
|
| 47 |
Disturbing the histone code in leukemia: translocations and mutations affecting histone methyl transferases
|
Chopra, Martin
|
|
2015
|
212-213 |
5 |
p. 192-205
14 p.
|
artikel
|
| 48 |
DNA methylation and RNA expression profiles in lung adenocarcinomas of never-smokers
|
Mansfield, Aaron S.
|
|
2015
|
212-213 |
5 |
p. 253-260
8 p.
|
artikel
|
| 49 |
Downregulation of miR-21 increases cisplatin sensitivity of non–small-cell lung cancer
|
Xu, Liyun
|
|
2014
|
212-213 |
5 |
p. 214-220
7 p.
|
artikel
|
| 50 |
Dystrophin and dysferlin double mutant mice: a novel model for rhabdomyosarcoma
|
Hosur, Vishnu
|
|
2012
|
212-213 |
5 |
p. 232-241
10 p.
|
artikel
|
| 51 |
Editorial Board
|
|
|
2014
|
212-213 |
5 |
p. IFC-
1 p.
|
artikel
|
| 52 |
Editorial Board
|
|
|
2016
|
212-213 |
5 |
p. CO2-
1 p.
|
artikel
|
| 53 |
Editorial Board
|
|
|
2015
|
212-213 |
5 |
p. IFC-
1 p.
|
artikel
|
| 54 |
Editorial Board
|
|
|
2013
|
212-213 |
5 |
p. IFC-
1 p.
|
artikel
|
| 55 |
Editorial Board
|
|
|
2012
|
212-213 |
5 |
p. IFC-
1 p.
|
artikel
|
| 56 |
Editorial Board
|
|
|
2011
|
212-213 |
5 |
p. IFC-
1 p.
|
artikel
|
| 57 |
Epigenetic changes in BRCA1-mutated familial breast cancer
|
Downs, Bradley
|
|
2015
|
212-213 |
5 |
p. 237-240
4 p.
|
artikel
|
| 58 |
Evaluation of a Cystic Placenta: Spectrum of Genomic Changes Including GRB10 Microdeletion
|
Surti, Urvashi
|
|
2016
|
212-213 |
5 |
p. 231-
1 p.
|
artikel
|
| 59 |
Evaluation of the Clinical Utility of Sanger Sequencing Following Next Generation Sequence Analysis
|
Sanmann, Jennifer N.
|
|
2016
|
212-213 |
5 |
p. 246-
1 p.
|
artikel
|
| 60 |
Exon-Targeted Array CGH for Identification of Clinically Relevant Small-Sized, Intragenic CNVs
|
Patel, Ankita
|
|
2016
|
212-213 |
5 |
p. 239-240
2 p.
|
artikel
|
| 61 |
Expression of HOXB genes is significantly different in acute myeloid leukemia with a partial tandem duplication of MLL vs. a MLL translocation: a cross-laboratory study
|
Liu, Hsi-Che
|
|
2011
|
212-213 |
5 |
p. 252-259
8 p.
|
artikel
|
| 62 |
Four Generation Family With a Complex Insertion of 16q in 4p
|
DuPont, Barbara R.
|
|
2016
|
212-213 |
5 |
p. 236-237
2 p.
|
artikel
|
| 63 |
Further evidence for germline BAP1 mutations predisposing to melanoma and malignant mesothelioma
|
Cheung, Mitchell
|
|
2013
|
212-213 |
5 |
p. 206-210
5 p.
|
artikel
|
| 64 |
Gamification of Chromosome Identification: Creation of a Software Tool to Introduce Cytogenetic Analysis
|
Paschal, Cate Randall
|
|
2016
|
212-213 |
5 |
p. 239-
1 p.
|
artikel
|
| 65 |
Genomic imbalances in benign metastasizing leiomyoma: characterization by conventional karyotypic, fluorescence in situ hybridization, and whole genome SNP array analysis
|
Bowen, Joslin M.
|
|
2012
|
212-213 |
5 |
p. 249-254
6 p.
|
artikel
|
| 66 |
Glioblastoma specimens with TP53 mutations do not show EGFRvIII amplification
|
Stoczynska-Fidelus, Ewelina
|
|
2011
|
212-213 |
5 |
p. 282-283
2 p.
|
artikel
|
| 67 |
High frequency of BTG1 deletions in patients with BCR-ABL1–positive acute leukemia
|
Xie, Jundan
|
|
2014
|
212-213 |
5 |
p. 226-230
5 p.
|
artikel
|
| 68 |
High Resolution Genomic Profiling of Metastatic Testicular Teratomas
|
Ouyang, Karen J.
|
|
2013
|
212-213 |
5 |
p. 213-
1 p.
|
artikel
|
| 69 |
High Resolution SNP Microarray Analysis is Useful for Diagnosis and Prognosis of Renal Epithelial Neoplasms
|
Wolff, Daynna J.
|
|
2013
|
212-213 |
5 |
p. 215-
1 p.
|
artikel
|
| 70 |
5-hydroxymethylcytosine in cancer: significance in diagnosis and therapy
|
Vasanthakumar, Aparna
|
|
2015
|
212-213 |
5 |
p. 167-177
11 p.
|
artikel
|
| 71 |
Hypermethylation of the CpG dinucleotide in epidermal growth factor receptor codon 790: implications for a mutational hotspot leading to the T790M mutation in non–small-cell lung cancer
|
Fujii, Akiko
|
|
2015
|
212-213 |
5 |
p. 271-278
8 p.
|
artikel
|
| 72 |
Identification of genetic susceptibility to childhood cancer through analysis of genes in parallel
|
|
|
2011
|
212-213 |
5 |
p. 284-
1 p.
|
artikel
|
| 73 |
Identification of the prevalent BRCA1 and BRCA2 mutations in the female population of Puerto Rico
|
Dutil, Julie
|
|
2012
|
212-213 |
5 |
p. 242-248
7 p.
|
artikel
|
| 74 |
Incidental Findings Found in Whole Genome SNP Microarray Analysis in Both Prenatal and Oncology Studies
|
Schwartz, Stuart
|
|
2016
|
212-213 |
5 |
p. 233-234
2 p.
|
artikel
|
| 75 |
Increased copy number of the DLX4 homeobox gene in breast axillary lymph node metastasis
|
Torresan, Clarissa
|
|
2014
|
212-213 |
5 |
p. 177-187
11 p.
|
artikel
|
| 76 |
Increased sperm aneuploidy in two male carriers of germline TP53 mutations
|
Paulasova, Petra
|
|
2011
|
212-213 |
5 |
p. 278-281
4 p.
|
artikel
|
| 77 |
Inheritance and Phase Determination in a Patient With Early Onset Parkinson Disease and Two PARK2 Deletions
|
Williams, Eli S.
|
|
2016
|
212-213 |
5 |
p. 240-
1 p.
|
artikel
|
| 78 |
Inhibition of the mevalonate pathway affects epigenetic regulation in cancer cells
|
Karlic, Heidrun
|
|
2015
|
212-213 |
5 |
p. 241-252
12 p.
|
artikel
|
| 79 |
Integrated high-resolution array CGH and SKY analysis of homozygous deletions and other genomic alterations present in malignant mesothelioma cell lines
|
Klorin, Geula
|
|
2013
|
212-213 |
5 |
p. 191-205
15 p.
|
artikel
|
| 80 |
Integrative analysis of copy number alteration and gene expression profiling in ovarian clear cell adenocarcinoma
|
Sung, Chang Ohk
|
|
2013
|
212-213 |
5 |
p. 145-153
9 p.
|
artikel
|
| 81 |
Interpreting Complex SNP-Array Results in Tumors: Clues Invoking Classical Cytogenetic Mechanisms
|
Rowsey, Ross A.
|
|
2016
|
212-213 |
5 |
p. 234-
1 p.
|
artikel
|
| 82 |
Introduction to progress and promise of epigenetics for diagnosis and therapy in cancer
|
Zeleznik-Le, Nancy J.
|
|
2015
|
212-213 |
5 |
p. 165-166
2 p.
|
artikel
|
| 83 |
Is Intrachromosomal Amplification of Chromosome 21 (iAMP21) Always Intrachromosomal?
|
Tsuchiya, Karen
|
|
2016
|
212-213 |
5 |
p. 231-232
2 p.
|
artikel
|
| 84 |
Isolated Sex Chromosome Loss after Allogeneic Stem Cell Transplant in Patients With Hematological Malignancies
|
Tang, Zhenya
|
|
2016
|
212-213 |
5 |
p. 241-
1 p.
|
artikel
|
| 85 |
It's Not You, It's Me: Somatic and Germline Mutations Detected Through Routine Clinical Testing
|
Morrissette, Jennifer
|
|
2016
|
212-213 |
5 |
p. 234-235
2 p.
|
artikel
|
| 86 |
Jumping-like translocation—a rare chromosomal rearrangement in a patient with Burkitt lymphoma/leukemia
|
Sarova, Iveta
|
|
2014
|
212-213 |
5 |
p. 221-225
5 p.
|
artikel
|
| 87 |
Massive Parallel Sequencing of Leukemia Samples Using a Custom Designed Cancer Gene Mutation Panel
|
Chang, Fengqi
|
|
2013
|
212-213 |
5 |
p. 211-
1 p.
|
artikel
|
| 88 |
Microarray Analysis of Formalin-Fixed Paraffin-Embedded (FFPET) and Frozen (FZT) Uveal Melanoma Detects Clinically Relevant Abnormalities, Including Chromosome 3 Loss of Heterozygosity
|
Schultz, Roger A.
|
|
2013
|
212-213 |
5 |
p. 214-
1 p.
|
artikel
|
| 89 |
Microarray and Next Generation Sequencing: Complementary Technologies for Diagnosing Autosomal Recessive Disorders
|
Chaubey, Alka
|
|
2016
|
212-213 |
5 |
p. 239-
1 p.
|
artikel
|
| 90 |
Microarray Studies in Pediatric T-Cell Acute Lymphoblastic Leukemia/Lymphoma: A Report of Four Cases
|
Sanmann, Jennifer N.
|
|
2013
|
212-213 |
5 |
p. 213-
1 p.
|
artikel
|
| 91 |
Microdeletion of ZBTB20 Results in a Phenotype Overlapping With That of the Microdeletion 3q13.31 Syndrome
|
Mulatinho, Milene
|
|
2016
|
212-213 |
5 |
p. 244-245
2 p.
|
artikel
|
| 92 |
MicroRNA profiling with correlation to gene expression revealed the oncogenic miR-17-92 cluster to be up-regulated in osteosarcoma
|
Baumhoer, Daniel
|
|
2012
|
212-213 |
5 |
p. 212-219
8 p.
|
artikel
|
| 93 |
Molecular characterization of a t(2;7) translocation linking CDK6 to the IGK locus in CD5− monoclonal B-cell lymphocytosis
|
Parker, Edward
|
|
2011
|
212-213 |
5 |
p. 260-264
5 p.
|
artikel
|
| 94 |
Molecular Inversion Probes for Detection of Copy Number Alterations and Loss of Heterozygosity in Renal Cell Carcinoma
|
Jobanputra, Vaidehi
|
|
2013
|
212-213 |
5 |
p. 212-
1 p.
|
artikel
|
| 95 |
Molecular pathology and its diagnostic use in bone tumors
|
Szuhai, Karoly
|
|
2012
|
212-213 |
5 |
p. 193-204
12 p.
|
artikel
|
| 96 |
Multiple CDK/CYCLIND genes are amplified in medulloblastoma and supratentorial primitive neuroectodermal brain tumor
|
Li, Meihua
|
|
2012
|
212-213 |
5 |
p. 220-231
12 p.
|
artikel
|
| 97 |
Mutation analysis of the PALB2 gene in unselected pancreatic cancer patients in the Czech Republic
|
Borecka, M.
|
|
2016
|
212-213 |
5 |
p. 199-204
6 p.
|
artikel
|
| 98 |
Mutation Profiling of Clinical Tumor Samples Using Next Generation Sequencing
|
Liu, Liu
|
|
2013
|
212-213 |
5 |
p. 213-
1 p.
|
artikel
|
| 99 |
MYC Gene Rearrangement in Plasma Cell Neoplasms
|
Biggerstaff, Julie Sanford
|
|
2016
|
212-213 |
5 |
p. 235-236
2 p.
|
artikel
|
| 100 |
New Genetic Alterations in Pediatric Acute Lymphoblastic Leukemia Uncovered by Chromosomal Microarray Analysis
|
Gaskin, Shannon
|
|
2016
|
212-213 |
5 |
p. 234-
1 p.
|
artikel
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| 101 |
Next Generation Cytogenetics: Genome-wide Mate Pair Sequencing for Detection of Structural Rearrangements and Copy Number Variation
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Aypar, Umut
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Next Generation Interphase Chromosome Profiling (NextGen ICP): Proof-of-Concept of Novel Technology
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Babu, Ramesh
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Non-Invasive Prenatal Screening of Over 200,000 Tests Performed at Natera
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Zneimer, Susan
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Novel Cytogenetic Findings in a Case of Mixed Phenotype Acute Leukemia With a Complex Karyotype
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Shabsovich, David
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Optimizing Array Design and Content for the Modern Cytogenetic Research Lab
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Chin, Ephrem
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Over-expression of prolyl hydroxylase-1 blocks NF-κB-mediated cyclin D1 expression and proliferation in lung carcinoma cells
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Xie, Xiao
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Pediatric leukemia predisposition syndromes: clues to understanding leukemogenesis
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Seif, Alix E.
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Performance of the Genomic DNA Assay for the Agilent 4200 TapeStation System
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Nitsche, Rainer
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Poly (AT) polymorphism in the XPC gene and smoking enhance the risk of prostate cancer in a low-risk Chinese population
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Liu, Yang
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Precision Medicine for Autism and Related Developmental Brain Disorders
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Predictive chromosomal clusters of synchronous and metachronous brain metastases in clear cell renal cell carcinoma
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Gutenberg, Angelika
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Prenatal SNP Microarray Analysis and Parental Follow-up of 16q24.1 Deletions That Include the FOXF1 Gene
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Schleede, Justin
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Pre-Phase Chemotherapy for Acute Lymphoblastic Leukemia: A Cautionary Tale
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Arreola, Alexandra
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Promoter hypermethylation of membrane type 3 matrix metalloproteinase is associated with cell migration in colorectal adenocarcinoma
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Moon, Ji Wook
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Publisher's note
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Ruimy, Anne
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Rare Focal Deletions Involving SNRPN and UBE3A Genes
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Meck, Jeanne
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Re-Examination of Danish Carriers of Balanced Chromosomal Inversions
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Regulatory Mutations of FOXG1 in the Context of Topological Domains
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Mehrjouy, Mana M.
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SH2B3 Aberrations Enriched in iAMP21 B Lymphoblastic Leukemia Cohort
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Baughn, Linda
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SOSTDC1 down-regulation of expression involves CpG methylation and is a potential prognostic marker in gastric cancer
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Gopal, Gopisetty
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Table of Contents
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Table of Contents
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Table of Contents
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Table of Contents
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2012
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Table of Contents
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Table of Contents
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The ABL and JAK Tyrosine Kinase Pathways May be Co-Activated in a Subset of BCR/ABL1 Positive Acute Lymphoid Leukemia
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Aviv, Hana
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The cancer COMPASS: navigating the functions of MLL complexes in cancer
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The Clinical Spectrum Associated With Xq25q26 Duplications: A Report of Two Novel Duplications and Review of the Literature
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The Effective Use of the Cancer Genome Atlas (TCGA) Data by the Cancer Cytogenetic Community
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Shams, Soheil
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The effect of TP53 codon 72 and RNASEL codon 462 polymorphisms on the development of cervical cancer in Argentine women
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The pathological role and prognostic impact of miR-181 in acute myeloid leukemia
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The potential utility of re-mining results of somatic mutation testing: KRAS status in lung adenocarcinoma
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The prognostic significance of an inv(3)(q21q26.2) in addition to a t(9;22)(q34;q11.2) in patients treated with tyrosine kinase inhibitors
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The role of the histone demethylase KDM4A in cancer
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The roles of chromatin-remodelers and epigenetic modifiers in kidney cancer
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The t(12;21) Translocation in the Context of a Complex Karyotype in Pediatric B-ALL
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The Use of Next Generation Sequencing in the Evaluation of Myeloid Neoplasms: A Comparison with Cytogenetics
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Title—TBD
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Triploidy in a Live-Born Female With Normal Non-Invasive Prenatal Testing Results
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Trisomy 12 and Triploidy in an Infant: An Unusual Case of Diploid/Triploid Mixoploidy
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Trisomy 12 Mosaicism Detected by Genomic Microarray in a Newborn Child
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Hong, Bo
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Two new Translocations Involving RUNX1
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Unexpected Chromosomal Abnormalities Identified by CMA Confirmation Studies
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Unique Challenges and Discoveries From Chromosome Genomic Array Testing (CGAT) in the Setting of Hematopoietic Cell Transplantation
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WEE1 is a validated target of the microRNA miR-17-92 cluster in leukemia
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What Elephants Can Teach Us About Preventing Cancer in Humans
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Whole-arm translocation of der(5;17)(p10;q10) with concurrent TP53 mutations in acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS): A unique molecular-cytogenetic subgroup
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Why Chromosomes Are Relevant
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Cherry, Athena M.
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