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                             31 gevonden resultaten
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
                             31 gevonden resultaten
 
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