| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Author index
|
|
|
2005
|
48 |
4 |
p. 553-555
3 p.
|
artikel
|
| 2 |
Contents
|
|
|
2005
|
48 |
4 |
p. 428-442
15 p.
|
artikel
|
| 3 |
CV2 Editorial Board redaction
|
|
|
2005
|
48 |
4 |
p. CO2-
1 p.
|
artikel
|
| 4 |
16: Evolution of novel genes and complex genome architecture by serial segmental duplication during primate speciation
|
Stankiewicz, Pawel
|
|
2005
|
48 |
4 |
p. 477-478
2 p.
|
artikel
|
| 5 |
Familial Mediterranean fever (FMF) in Lebanon and Jordan: a population genetics study and report of three novel mutations
|
Medlej-Hashim, Myrna
|
|
2005
|
48 |
4 |
p. 412-420
9 p.
|
artikel
|
| 6 |
FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype
|
Baroncini, Anna
|
|
2005
|
48 |
4 |
p. 388-396
9 p.
|
artikel
|
| 7 |
Hyperechogenic fetal bowel: counseling difficulties
|
Marcus-Soekarman, D.
|
|
2005
|
48 |
4 |
p. 421-425
5 p.
|
artikel
|
| 8 |
I2: Advanced single cell analysis
|
Speicher, Michael
|
|
2005
|
48 |
4 |
p. 456-
1 p.
|
artikel
|
| 9 |
I7: Applications of genomic micro-arrays in research and diagnostics of central nervous system tumors
|
Dumanski, Jan
|
|
2005
|
48 |
4 |
p. 481-484
4 p.
|
artikel
|
| 10 |
I3: DECIPHER
|
Carter, Nigel
|
|
2005
|
48 |
4 |
p. 466-
1 p.
|
artikel
|
| 11 |
I11: Dynamics of DNA double-strand breaks revealed by clustering of damaged chromosome domains
|
Aten, Jacob A.
|
|
2005
|
48 |
4 |
p. 537-
1 p.
|
artikel
|
| 12 |
I10: Identification of prognostic markers in brain tumors
|
Radlwimmer, Bernhard
|
|
2005
|
48 |
4 |
p. 484-
1 p.
|
artikel
|
| 13 |
I9: Micro-arrays consisting of pooled BACs for rapid detection of genomic imbalances
|
Szuhai, Karoly
|
|
2005
|
48 |
4 |
p. 529-
1 p.
|
artikel
|
| 14 |
I1: Molecular mechanisms for rearrangements and their conveyed phenotypes in genomic disorders
|
Bi, Weimin
|
|
2005
|
48 |
4 |
p. 443-
1 p.
|
artikel
|
| 15 |
I8: Oligo array CGH a fast, sensitive and high resolution platform
|
Ylstra, Bauke
|
|
2005
|
48 |
4 |
p. 528-529
2 p.
|
artikel
|
| 16 |
I4: Segmental duplications: a bioinformatics point of view
|
Eichler, Evan
|
|
2005
|
48 |
4 |
p. 466-
1 p.
|
artikel
|
| 17 |
Keyword index
|
|
|
2005
|
48 |
4 |
p. 557-564
8 p.
|
artikel
|
| 18 |
List of Participants
|
|
|
2005
|
48 |
4 |
p. 543-552
10 p.
|
artikel
|
| 19 |
2nd Marie Curie Conference on arrayCGH and Molecular Cytogenetics
|
Speleman, Frank
|
|
2005
|
48 |
4 |
p. 426-427
2 p.
|
artikel
|
| 20 |
Neuropathic visceral dysmotility, brain cysts and calcifications, facial dysmorphism and developmental delay in two sibs. A new syndrome?
|
Hadchouel, Alice
|
|
2005
|
48 |
4 |
p. 367-376
10 p.
|
artikel
|
| 21 |
Novel GJA1 mutations in patients with oculo-dento-digital dysplasia (ODDD)
|
Debeer, Ph.
|
|
2005
|
48 |
4 |
p. 377-387
11 p.
|
artikel
|
| 22 |
O34: Absolute fluorescence calibration
|
Young, Ian T.
|
|
2005
|
48 |
4 |
p. 533-
1 p.
|
artikel
|
| 23 |
O21: Amplification and instability of chromosome 21 in patients with ALL identified with BAC and oligonucleotide-based array CGH (aCGH)
|
Strefford, Jon C.
|
|
2005
|
48 |
4 |
p. 488-489
2 p.
|
artikel
|
| 24 |
O11: Analysis of array CGH experiments: methods for the identification of informative genomic alterations
|
Hupé, Philippe
|
|
2005
|
48 |
4 |
p. 467-468
2 p.
|
artikel
|
| 25 |
O24: Analysis of ependymal neoplasms by DNA-copy number and protein expression profiling
|
Mendrzyk, Frank
|
|
2005
|
48 |
4 |
p. 491-492
2 p.
|
artikel
|
| 26 |
O25: Analysis of the genetic similarity of 10 cancer types using genome copy number data
|
Greshock, Joel
|
|
2005
|
48 |
4 |
p. 492-493
2 p.
|
artikel
|
| 27 |
O22: A new recurrent 9q34 duplication in pediatric T-cell acute lymphoblastic leukemia
|
Van Vlierberghe, Pieter
|
|
2005
|
48 |
4 |
p. 490-
1 p.
|
artikel
|
| 28 |
O10: An improved algorithm for segmenting array-CGH data
|
Marioni, John C.
|
|
2005
|
48 |
4 |
p. 466-467
2 p.
|
artikel
|
| 29 |
O6: Array-based comparative genomic hybridization of single cells
|
Fuhrmann, Christine
|
|
2005
|
48 |
4 |
p. 456-
1 p.
|
artikel
|
| 30 |
O3: Array CGH findings in a large series of 150 patients with idiopathic mental retardation and congenital anomalies: unexpected findings and implications for future routine diagnostic screening
|
Menten, Björn
|
|
2005
|
48 |
4 |
p. 445-446
2 p.
|
artikel
|
| 31 |
O9: Array CGH using microdissected chromosomes to map chromosomal breakpoints
|
Backx, Liesbeth F.P.
|
|
2005
|
48 |
4 |
p. 458-459
2 p.
|
artikel
|
| 32 |
O8: Array CGH Using Whole Genome Amplification Of Fresh Frozen And Formalin-Fixed, Paraffin-Embedded Tumour DNA
|
Little, Suzanne
|
|
2005
|
48 |
4 |
p. 457-458
2 p.
|
artikel
|
| 33 |
O31: Array-MAPH: a novel microarray technology for genomic analysis
|
Kousoulidou, Ludmila
|
|
2005
|
48 |
4 |
p. 530-531
2 p.
|
artikel
|
| 34 |
O13: Automatic Identification of Chromosomal Aberrations in array-CGH Based Experiments Applying the ChipYard Framework for Microarray Data Analysis
|
Toedt, Grischa
|
|
2005
|
48 |
4 |
p. 469-470
2 p.
|
artikel
|
| 35 |
O17: Characterization of primary gastric tumors with CGH and expression microarray analyses
|
Junnila, Siina
|
|
2005
|
48 |
4 |
p. 485-486
2 p.
|
artikel
|
| 36 |
O5: Characterization of subtle copy number changes on the X chromosome identified in 7% of patients with X-linked mental retardation by high-resolution array-CGH
|
Bauters, Marijke
|
|
2005
|
48 |
4 |
p. 447-
1 p.
|
artikel
|
| 37 |
O38: Chromosome territory architecture in nuclei of human fibroblasts and lymphocytes
|
Küpper, Katrin
|
|
2005
|
48 |
4 |
p. 539-540
2 p.
|
artikel
|
| 38 |
O26: Combined arrayCGH and gene expression profiling delineates clinico-genetic subgroups and identifies rare amplicons encoding neuronal developmental genes
|
Michels, Evi
|
|
2005
|
48 |
4 |
p. 493-494
2 p.
|
artikel
|
| 39 |
O19: Construction and validation of a genomic BAC array with complete and tiling coverage of the human genome
|
Jönsson, Göran
|
|
2005
|
48 |
4 |
p. 487-
1 p.
|
artikel
|
| 40 |
Oculo-auriculo-vertebral spectrum (OAVS): clinical evaluation and severity scoring of 53 patients and proposal for a new classification
|
Tasse, Christiane
|
|
2005
|
48 |
4 |
p. 397-411
15 p.
|
artikel
|
| 41 |
O29: Detailed characterization of MYC-containing double minutes in hematologic malignancies: exclusion of MYC as the target gene and evidence in favor of an episome model in the genesis of dmin
|
Storlazzi, Clelia T.
|
|
2005
|
48 |
4 |
p. 495-496
2 p.
|
artikel
|
| 42 |
O4: Detection of structural low-grade mosaicism by array CGH
|
Thienpont, Bernard
|
|
2005
|
48 |
4 |
p. 446-447
2 p.
|
artikel
|
| 43 |
O2: Diagnosis of genetic abnormalities in developmentally delayed patients: a new strategy combining MLPA and arrayCGH
|
Knijnenburg, Jeroen
|
|
2005
|
48 |
4 |
p. 444-445
2 p.
|
artikel
|
| 44 |
O20: Discovering genetic profiles by array-CGH in familial breast tumors
|
van Beers, Erik H.
|
|
2005
|
48 |
4 |
p. 487-488
2 p.
|
artikel
|
| 45 |
O14: Evolutionary centromere repositioning
|
Ventura, Mario
|
|
2005
|
48 |
4 |
p. 478-
1 p.
|
artikel
|
| 46 |
O16: Few duplicons make the most noise
|
Pramparo, Tiziano
|
|
2005
|
48 |
4 |
p. 479-480
2 p.
|
artikel
|
| 47 |
O28: Genome position effects on gene amplification
|
Gajduskova, Pavla
|
|
2005
|
48 |
4 |
p. 495-
1 p.
|
artikel
|
| 48 |
O33: Genome wide copy number analysis of 1 ng of genomic DNA using a random primer amplification and labeling method
|
Vandesompele, Jo
|
|
2005
|
48 |
4 |
p. 532-533
2 p.
|
artikel
|
| 49 |
O23: Genomic profile of CML by aCGH
|
Nacheva, Elisabeth P.
|
|
2005
|
48 |
4 |
p. 490-491
2 p.
|
artikel
|
| 50 |
O27: Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution BAC microarrays
|
Heidenblad, Markus
|
|
2005
|
48 |
4 |
p. 494-495
2 p.
|
artikel
|
| 51 |
O32: Genotyping single DNA molecules in situ
|
Nilsson, Mats
|
|
2005
|
48 |
4 |
p. 532-
1 p.
|
artikel
|
| 52 |
O37: Histone lysine methylation patterns in human cell types are arranged in distinct three-dimensional nuclear zones
|
Albiez, Heiner
|
|
2005
|
48 |
4 |
p. 538-539
2 p.
|
artikel
|
| 53 |
O30: Human chromosome 1 methylation profiling reveals regional differences among tissues
|
De Bustos, Cecilia
|
|
2005
|
48 |
4 |
p. 529-530
2 p.
|
artikel
|
| 54 |
O15: Identification of large-scale human-specific copy number variations by array comparative genomic hybridization
|
Goidts, Violaine
|
|
2005
|
48 |
4 |
p. 478-479
2 p.
|
artikel
|
| 55 |
O35: New chromosome nomenclature based on DNA sequence information
|
Ambros, Peter F.
|
|
2005
|
48 |
4 |
p. 533-534
2 p.
|
artikel
|
| 56 |
O36: Replication timing dependent spatial chromatin arrangements in hominoid primates
|
Grasser, Florian
|
|
2005
|
48 |
4 |
p. 537-538
2 p.
|
artikel
|
| 57 |
O7: Single cell aneuploidy detection by array CGH
|
Le Caignec, Cedric
|
|
2005
|
48 |
4 |
p. 456-457
2 p.
|
artikel
|
| 58 |
O12: Text Mining for Constitutional Cytogenetics
|
Van Vooren, Steven W.
|
|
2005
|
48 |
4 |
p. 468-469
2 p.
|
artikel
|
| 59 |
O18: Tiling path array CGH of breast cancer cell lines and integration with expression profiling
|
Mackay, Alan
|
|
2005
|
48 |
4 |
p. 486-487
2 p.
|
artikel
|
| 60 |
O1: Tiling resolution genome profiling in mental retardation
|
de Vries, Bert B.
|
|
2005
|
48 |
4 |
p. 444-
1 p.
|
artikel
|
| 61 |
P37: A combined FISH and array CGH study shows great complexity of chromosomal rearrangements on 8p12 in breast, colon and pancreatic cancer cell lines
|
Pole, Jessica C.
|
|
2005
|
48 |
4 |
p. 502-503
2 p.
|
artikel
|
| 62 |
P34: Analysing DNA copy number changes in lung carcinomas and adjacent bronchial epithelium by means of high-resolution array CGH
|
Muradyan, Artur
|
|
2005
|
48 |
4 |
p. 500-501
2 p.
|
artikel
|
| 63 |
P75: Analysis of expression related changes of a Tat inducible HIV construct
|
Weierich, Claudia
|
|
2005
|
48 |
4 |
p. 541-
1 p.
|
artikel
|
| 64 |
P16: Aneuploidy-screening in single cells by a rapid comparative genomic hybridization protocol for prenatal diagnostics
|
Landwehr, Christina
|
|
2005
|
48 |
4 |
p. 462-
1 p.
|
artikel
|
| 65 |
P21: A new generation genome viewers for molecular cytogenetics
|
Eussen, Bert
|
|
2005
|
48 |
4 |
p. 470-
1 p.
|
artikel
|
| 66 |
P74: Arrangements of chromosome territories in human cell clones
|
Köhler, Daniela
|
|
2005
|
48 |
4 |
p. 540-541
2 p.
|
artikel
|
| 67 |
P17: Array-based comparative genomic hybridization of laser-microdissected epithelia from formalin fixed and paraffin embedded breast and prostate tissue
|
Montag, Ulrike
|
|
2005
|
48 |
4 |
p. 462-463
2 p.
|
artikel
|
| 68 |
P28: array-CGHbase V2: an analysis platform for expression, CGH and SNP microarrays
|
Menten, Björn
|
|
2005
|
48 |
4 |
p. 475-476
2 p.
|
artikel
|
| 69 |
P26: Array-CGH data processing and presentation
|
Nacheva, Elisabeth P.
|
|
2005
|
48 |
4 |
p. 474-
1 p.
|
artikel
|
| 70 |
P3: Array-CGH for the identification of autism susceptibility loci
|
Mansouri, Mahmoud
|
|
2005
|
48 |
4 |
p. 449-450
2 p.
|
artikel
|
| 71 |
P41: Array-comparative genomic hybridisation identifies specific rearrangement in atypical lipomatous tumour/well-differentiated liposarcoma and improves the diagnosis
|
Szuhai, Karoly
|
|
2005
|
48 |
4 |
p. 505-506
2 p.
|
artikel
|
| 72 |
P14: Array comparative genomic hybridization: parameters affecting the quality using low amount of starting material
|
van der Burg, Marja J.
|
|
2005
|
48 |
4 |
p. 460-461
2 p.
|
artikel
|
| 73 |
P24: Array Pipeline: A Dedicated Laboratory Information Management System and Associated Software Utilities for CGH-Microarray Manufacture and Analysis
|
Jones, Christopher
|
|
2005
|
48 |
4 |
p. 472-473
2 p.
|
artikel
|
| 74 |
P59: Breast cancer genomics reveals highly complex rearrangement patterns and opens the question of what events are essential
|
Orsetti, B
|
|
2005
|
48 |
4 |
p. 519-520
2 p.
|
artikel
|
| 75 |
P31: Breast tumors induced by high dose radiation display similar genetic profiles
|
Broeks, Annegien
|
|
2005
|
48 |
4 |
p. 497-498
2 p.
|
artikel
|
| 76 |
P64: Can molecular cytogenetics predict the outcome of patients with multiple myeloma?
|
Castellanos, Mariana
|
|
2005
|
48 |
4 |
p. 523-524
2 p.
|
artikel
|
| 77 |
P23: CAP: a Web-based platform for CGH-array management and analysis
|
La Rosa, Philippe
|
|
2005
|
48 |
4 |
p. 471-472
2 p.
|
artikel
|
| 78 |
P51: Chromosomal aberrations in oral squamous cell carcinomas by μarray comparative genomic hybridizations
|
Roman, Eric
|
|
2005
|
48 |
4 |
p. 513-514
2 p.
|
artikel
|
| 79 |
P60: Chromosomal imbalances detected by CGH-array in B-cell splenic marginal zone lymphomas (SMZL)
|
Robledo, Cristina
|
|
2005
|
48 |
4 |
p. 520-521
2 p.
|
artikel
|
| 80 |
P30: Chromosome 22 array-CGH profiling of breast cancer reveals tumor heterogeneity and 340 kb shared region of loss with ovarian cancer
|
Benetkiewicz, Magdalena
|
|
2005
|
48 |
4 |
p. 496-497
2 p.
|
artikel
|
| 81 |
P62: Classical cytogenetics, interphase FISH and SKY contribution in childhood acute myeloid leukemia
|
Jeison, Marta
|
|
2005
|
48 |
4 |
p. 522-523
2 p.
|
artikel
|
| 82 |
P65: Complete imatinib-induced CML remission as evidenced by FISH predicts good outcome but it is not achieved in patients with der(9) deletion within 18-month follow up
|
Fantasia, Donatella
|
|
2005
|
48 |
4 |
p. 524-525
2 p.
|
artikel
|
| 83 |
P45: Comprehensive genomic analysis of desmoplastic medulloblastomas reveals novel amplified genes and supports a monoclonal origin of the different histologic components
|
Hoischen, Alexander
|
|
2005
|
48 |
4 |
p. 509-
1 p.
|
artikel
|
| 84 |
P25: Computational Aspects of Large Scale Cytogenetic Data Mining
|
Baudis, Michael
|
|
2005
|
48 |
4 |
p. 473-474
2 p.
|
artikel
|
| 85 |
P44: Conventional and 1p-specific microarray-based CGH analysis of sporadic and syndrome-related pheochromocytomas
|
Speel, Ernst-Jan M.
|
|
2005
|
48 |
4 |
p. 508-
1 p.
|
artikel
|
| 86 |
P54: Correlation of the copy number DNA aberration pattern in gastrointestinal stromal tumors (GISTs) with tumor genotype and anatomic site
|
Wozniak, Agnieszka
|
|
2005
|
48 |
4 |
p. 516-517
2 p.
|
artikel
|
| 87 |
P1: Detailed molecular characterization of a Swedish cohort of Cornelia de Lange syndrome patients
|
Schoumans, Jacqueline
|
|
2005
|
48 |
4 |
p. 447-448
2 p.
|
artikel
|
| 88 |
P12: Detecting single DNA copy number variations in complex genomes using one nanogram of starting DNA and BAC-array CGH
|
Guillaud-Bataille, Marine
|
|
2005
|
48 |
4 |
p. 459-
1 p.
|
artikel
|
| 89 |
P6: Detection of pathologic and polymorphic cryptic chromosomal imbalances by array-CGH using a BAC-array targeting regions between segmental duplications
|
González, Eva
|
|
2005
|
48 |
4 |
p. 451-452
2 p.
|
artikel
|
| 90 |
P38: DNA copy number changes predicting resistance to therapy in ovarian cancer patients
|
Garcia, Maria J.
|
|
2005
|
48 |
4 |
p. 503-504
2 p.
|
artikel
|
| 91 |
P27: Dynamic filtering and transformation of microarray data
|
Brooks, Peter
|
|
2005
|
48 |
4 |
p. 474-475
2 p.
|
artikel
|
| 92 |
P71: Dy415-ULS labeled probes, new blue fluorescent probes for FISH
|
van Gijlswijk, Rob
|
|
2005
|
48 |
4 |
p. 535-
1 p.
|
artikel
|
| 93 |
P56: Epigenetic profiling by semi-quantitative comparative hybridization of digested and undigested tumor DNA on a 11.2K CpG island microarray
|
Schlaeger, Christof
|
|
2005
|
48 |
4 |
p. 517-518
2 p.
|
artikel
|
| 94 |
P2: Finetuning of the genotype-phenotype correlation in Cri du Chat syndrome using array CGH
|
Mul, Adri
|
|
2005
|
48 |
4 |
p. 448-449
2 p.
|
artikel
|
| 95 |
P35: Frequent loss of chromosome 1p and 22q loci in insulinomas
|
Jonkers, Yvonne M.H.
|
|
2005
|
48 |
4 |
p. 501-
1 p.
|
artikel
|
| 96 |
P29: From “chromosome painting” to “array painting” to identify the evolutionarym breakpoint sequences in Hylobates karyotypes
|
Carbone, Lucia
|
|
2005
|
48 |
4 |
p. 480-481
2 p.
|
artikel
|
| 97 |
P61: Genetic aberrations in hairy cell leukemia demonstrated by arrayCGH and FISH analysis
|
Pospisilova, Helena
|
|
2005
|
48 |
4 |
p. 521-522
2 p.
|
artikel
|
| 98 |
P5: Genome-wide array-CGH screening of 52 patients with idiopathic mental retardation – Detection of two cases with de novo imbalances and two cases with causative imbalances inherited from a parent
|
Ehrbrecht, Antje
|
|
2005
|
48 |
4 |
p. 450-451
2 p.
|
artikel
|
| 99 |
P58: Genome-wide SNP microarray analysis to detect copy number changes acquired isodisomy: a proof-of-principle study
|
McMullan, Dom
|
|
2005
|
48 |
4 |
p. 519-
1 p.
|
artikel
|
| 100 |
P32: Genomic aberrations in tamoxifen-induced uterine malignancies following breast cancer
|
Fles, Renske
|
|
2005
|
48 |
4 |
p. 498-499
2 p.
|
artikel
|
| 101 |
P43: Genomic changes in favourable histology Wilms tumours analysed by genome-wide 1 Mb-spaced and chromosome 1 tiling-path array CGH
|
Natrajan, Rachael
|
|
2005
|
48 |
4 |
p. 507-508
2 p.
|
artikel
|
| 102 |
P47: Genomic profiling of renal cell carcinomas with loss of chromosome 3p
|
Kuiper, Roland
|
|
2005
|
48 |
4 |
p. 510-
1 p.
|
artikel
|
| 103 |
P13: GenomiPhi: A potential alternative to DOP-PCR in array construction?
|
Cooke, S.L.
|
|
2005
|
48 |
4 |
p. 460-
1 p.
|
artikel
|
| 104 |
P8: Genotype-phenotype correlation using high resolution karyotype, FISH studies, QF-PCR and micro-array CGH analysis of the first reported case of subtelomere deletion 12q
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Jean, Gekas
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2005
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48 |
4 |
p. 453-454
2 p.
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artikel
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| 105 |
P46: High-resolution analysis of copy number alterations in cancer using 44K CGH oligo microarrays
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Järvinen, Anna-Kaarina
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2005
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48 |
4 |
p. 509-510
2 p.
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artikel
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| 106 |
P33: High-resolution array-CGH profiling of chromosome 22 in patients affected with schwannomas
|
Hansson, Caisa M.
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2005
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48 |
4 |
p. 499-500
2 p.
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artikel
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| 107 |
P10: High resolution fine mapping of an extremely complex intrachromosomal rearrangement of chromosome 1 involving 13 breakpoints
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Sahlén, Sigrid
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2005
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48 |
4 |
p. 454-455
2 p.
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artikel
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| 108 |
P42: High resolution genomic profiling reveals association of chromosomal aberrations on 1q and 16p with histological and genetic subgroups of invasive breast cancer
|
Stange, Daniel E.
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2005
|
48 |
4 |
p. 506-507
2 p.
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artikel
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| 109 |
P40: Identification of chromosomal breakpoints in the radiation-transformed tumorigenic epithelial breast cell lines B42 by positional cloning and array painting
|
Unger, Kristian
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2005
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48 |
4 |
p. 505-
1 p.
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artikel
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| 110 |
P69: Identification of genes in neuroendocrine tumor development using microarray-CGH
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Hashemi, Jamileh
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2005
|
48 |
4 |
p. 527-528
2 p.
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artikel
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| 111 |
P66: Identification of genes involved in T-cell oncogenesis through FISH screening of TCR rearrangements in T-ALL
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Van Roy, N
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2005
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48 |
4 |
p. 525-526
2 p.
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artikel
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| 112 |
P68: Identification of genetic markers in radiotherapy-resistant head and neck cancers
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Bauer, Verena
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2005
|
48 |
4 |
p. 527-
1 p.
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artikel
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| 113 |
P49: Identification of recurrent chromosomal aberrations in different types of human germ cell tumours using array CGH
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Veltman, Imke
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2005
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48 |
4 |
p. 511-512
2 p.
|
artikel
|
| 114 |
P55: Identifying genomic imbalances in cervical lesions with array-based comparative genomic hybridization
|
Ng, Grace
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|
2005
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48 |
4 |
p. 517-
1 p.
|
artikel
|
| 115 |
P73: Impact of primate evolutionary chromosome rearrangements on the nuclear topology of genomic signatures
|
Neusser, Michaela
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|
2005
|
48 |
4 |
p. 540-
1 p.
|
artikel
|
| 116 |
P20: Improving Whole Genome Amplification methods for pre-implantation diagnosis
|
Nilsson, P.R.
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2005
|
48 |
4 |
p. 465-
1 p.
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artikel
|
| 117 |
P76: Kissing not required for maintenance of imprinting in cycling human cells
|
Teller, Kathrin
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|
2005
|
48 |
4 |
p. 541-542
2 p.
|
artikel
|
| 118 |
P19: LDASS: a novel PCR-based amplification and labelling method for detection of genomic copy number changes using minute amounts of DNA
|
De Preter, Katleen
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|
2005
|
48 |
4 |
p. 464-465
2 p.
|
artikel
|
| 119 |
P11: Loci of shared segmental aneuploidy in the genomes of healthy and mentally retarded subjects detected by Array-CGH
|
Poot, Martin
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|
2005
|
48 |
4 |
p. 455-
1 p.
|
artikel
|
| 120 |
P22: MAPH Designer – a web-based program for designing hybridization probes for the new array-MAPH method and array-CGH
|
Palta, Priit
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|
2005
|
48 |
4 |
p. 470-471
2 p.
|
artikel
|
| 121 |
P52: Microarray-CGH analysis of the 8q22–q23, 13q21–q31 and 20q amplicons associated with colorectal cancer progression
|
Carvalho, Beatriz
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|
2005
|
48 |
4 |
p. 514-515
2 p.
|
artikel
|
| 122 |
P9: Molecular cytogenetic mapping of an interstitial deletion of 10p in a patient with mild mental retardation, autistic features and facial dysmorphia
|
Rack, K.
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2005
|
48 |
4 |
p. 454-
1 p.
|
artikel
|
| 123 |
P63: Molecular karyotyping of a chondroblastoma to identify the new formed chimera-gene
|
IJszenga, Marije J.
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2005
|
48 |
4 |
p. 523-
1 p.
|
artikel
|
| 124 |
P48: New subgroups of high grade gliomas assessed by comparative genomic hybridization (CGH) and gene expression profile (GEP)
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Garcia, Juan L.
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2005
|
48 |
4 |
p. 511-
1 p.
|
artikel
|
| 125 |
P70: Oligo-based array CGH; a highly sensitive, reproducible and affordable option
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van den IJssel, Paul
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|
2005
|
48 |
4 |
p. 534-535
2 p.
|
artikel
|
| 126 |
P57: Overlapping amplified 3q28 region in COMA cell line and malignant fibrous histiocytoma primary tumors
|
Hussenet, Thomas
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|
2005
|
48 |
4 |
p. 518-519
2 p.
|
artikel
|
| 127 |
P15: Preimplantation genetic diagnosis for dystrophin gene deletions using fluorescence in situ hybridisation on single cells
|
Malmgren, Helena
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|
2005
|
48 |
4 |
p. 461-462
2 p.
|
artikel
|
| 128 |
P50: Profiling DNA copy number changes in sarcomas by array comparative genomic hybridisation
|
Meza-Zepeda, Leonardo A.
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|
2005
|
48 |
4 |
p. 512-513
2 p.
|
artikel
|
| 129 |
P36: Study of genetic pattern in BRCAx hereditary breast tumors by CGH
|
Chiarappa, Patrizia
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|
2005
|
48 |
4 |
p. 501-502
2 p.
|
artikel
|
| 130 |
P7: The application of a 6 K genome-wide BAC-array in clinical diagnostic
|
Kok, Klaas
|
|
2005
|
48 |
4 |
p. 452-453
2 p.
|
artikel
|
| 131 |
P67: The identification of common genetic alterations using array CGH to predict a response to radiotherapy in laryngeal carcinomas
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Gibcus, Johan
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|
2005
|
48 |
4 |
p. 526-527
2 p.
|
artikel
|
| 132 |
P53: Toward refinement of rhabdomyosarcoma classification by array CGH
|
Thuille, Bénédicte
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2005
|
48 |
4 |
p. 515-516
2 p.
|
artikel
|
| 133 |
P4: Ulnar-mammary syndrome with mental retardation caused by a novel 0.8 Mb deletion encompassing the TBX3 gene
|
Klopocki, Eva
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|
2005
|
48 |
4 |
p. 450-
1 p.
|
artikel
|
| 134 |
P39: Use of array painting to detect balanced translocations in breast cancer
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Howarth, Karen
|
|
2005
|
48 |
4 |
p. 504-505
2 p.
|
artikel
|
| 135 |
P18: Utilization of GenomiPhi, a whole genome amplification kit for Array-CGH
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Dhulipala, Prasad D.
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|
2005
|
48 |
4 |
p. 463-464
2 p.
|
artikel
|
| 136 |
P72: Validation of a new chromosome mapping tool by BAC clone hybridization to chromosomes stained with a base pair specific fluorochrome
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Kowalska, Agata
|
|
2005
|
48 |
4 |
p. 536-
1 p.
|
artikel
|
| 137 |
15: Structural variation of the human genome
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Eichler, Evan E.
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|
2005
|
48 |
4 |
p. 477-
1 p.
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