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Rapid and novel prenatal molecular assay for detecting aneuploidies and microdeletion syndromesGROSS, Susan J; BAJAJ, Komal; GARRY, David et al.Prenatal diagnosis. 2011, Vol 31, Num 3, pp 259-266, issn 0197-3851, 8 p.Article

Small regions of overlapping deletions on 6q26 in human astrocytic tumours identified using chromosome 6 tile path array-CGHICHIMURA, K; MUNGALL, A. J; FIEGLER, H et al.Oncogene (Basingstoke). 2006, Vol 25, Num 8, pp 1261-1271, issn 0950-9232, 11 p.Article

Chromosome aberrations evaluated by comparative genomic hybridization in B-cell chronic lymphocytic leukemia: correlation with CD38 expressionOITAGGIO, Laura; VIAGGI, Silvia; ZUNINO, Annalisa et al.Haematologica (Roma). 2003, Vol 88, Num 7, pp 769-777, issn 0390-6078, 9 p.Article

A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1-evidence for high variability in mosaicism in different tissues of sSMC carriersFICKELSCHER, Ina; STARKE, Heike; SCHULZE, Eberhard et al.Prenatal diagnosis. 2007, Vol 27, Num 8, pp 783-785, issn 0197-3851, 3 p.Article

Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMCLIEHR, Thomas; STARKE, Heike; SENGER, Gabriele et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 1, pp 46-51, issn 1552-4825, 6 p.Article

Genetic abnormalities associated with nodal metastasis in head and neck cancerWREESMANN, Volkert B; WANG, Dorothy; GOBERDHAN, Andy et al.Head & neck. 2004, Vol 26, Num 1, pp 10-15, issn 1043-3074, 6 p.Article

Quantification of fetal nucleated cells in maternal blood of pregnant women with a male trisomy 21 fetus using molecular cytogenetic techniquesKRABCHI, Kada; GADJI, Macoura; SAMASSEKOU, Oumar et al.Prenatal diagnosis. 2006, Vol 26, Num 1, pp 28-34, issn 0197-3851, 7 p.Article

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Genomic analysis of prostate carcinoma specimens obtained via ultrasound-guided needle biopsy may be of use in preoperative decision-makingTEIXEIRA, Manuel R; RIBEIRO, Franclim R; EKNAES, Mette et al.Cancer. 2004, Vol 101, Num 8, pp 1786-1793, issn 0008-543X, 8 p.Article

The Identification of Microdeletion Syndromes and Other Chromosome Abnormalities : Cytogenetic Methods of the Past, New Technologies for the FutureSHAFFER, Lisa G; BEJJANI, Bassem A; TORCHIA, Beth et al.American journal of medical genetics. Part C, Seminars in medical genetics. 2007, Vol 145, Num 4, pp 335-345, issn 1552-4868, 11 p.Article

Prenatal diagnosis and molecular cytogenetic characterisation of a small de novo interstitial duplication 16q11.2-q13TRIMBORN, Marc; WEGNER, Rolf-Dieter; TÖNNIES, Holger et al.Prenatal diagnosis. 2006, Vol 26, Num 3, pp 273-276, issn 0197-3851, 4 p.Article

MALT lymphoma with t(14;18)(q32;q21)/IGH-MALTI is characterized by strong cytoplasmic MALTI and BCL10 expressionHONGTAO YE; LIPING GONG; MARTIN-SUBERO, Jose I et al.Journal of pathology. 2005, Vol 205, Num 3, pp 293-301, issn 0022-3417, 9 p.Article

Establishment of a novel human dedifferentiated liposarcoma cell line, FU-DDLSs-1: Conventional and molecular cytogenetic characterizationNISHIO, Jun; IWASAKI, Hiroshi; ISHIGURO, Masako et al.International journal of oncology. 2003, Vol 22, Num 3, pp 535-542, issn 1019-6439, 8 p.Article

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Genetic aberrations in prostate cancer by microarray analysisSARAMÄKI, Outi R; PORKKA, Kati P; VESSELLA, Robert L et al.International journal of cancer. 2006, Vol 119, Num 6, pp 1322-1329, issn 0020-7136, 8 p.Article

G-banding and molecular cytogenetic analyses of marginal zone lymphomaAAMOT, Hege Vangstein; MICCI, Francesca; HOLTE, Harald et al.British journal of haematology. 2005, Vol 130, Num 6, pp 890-901, issn 0007-1048, 12 p.Article

Molecular characterization of a 14q deletion in a boy with features of holt-oram syndromeLE MEUR, Nathalie; GOLDENBERG, Alice; KLEINFINGER, Pascale et al.American journal of medical genetics. 2005, Vol 134A, Num 4, pp 439-442, issn 0148-7299, 4 p.Article

Advances in molecular cytogenetics for the evaluation of mental retardationJIE XU; ZHONG CHEN.American journal of medical genetics. 2003, Vol 117C, Num 1, pp 15-24, issn 0148-7299, 10 p.Article

Genome-wide copy number profiling on high-density bacterial artificial chromosomes, single-nucleotide polymorphisms, and oligonucleotide microarrays: A platform comparison based on statistical power analysisHEHIR-KWA, Jayne Y; EGMONT-PETERSEN, Michael; JANSSEN, Irene M et al.DNA research. 2007, Vol 14, Num 1, pp 1-11, issn 1340-2838, 11 p.Article

5. Molecular cytogenetic analysis of carcinomas of the digestive organs and its clinical application : Molecular approach for pathophysiology of digestive diseasesSASAKI, Kohsuke.Internal medicine (Tokyo. 1992). 2003, Vol 42, Num 3, pp 292-294, issn 0918-2918, 3 p.Article

Screening of genomic imbalances in glioblastoma multiforme using high-resolution comparative genomic hybridizationVRANOVA, Vladimira; NECESALOVA, Eva; KUGLIK, Petr et al.Oncology reports. 2007, Vol 17, Num 2, pp 457-464, issn 1021-335X, 8 p.Article

Establishment of a new human epithelioid sarcoma cell line, FU-EPS-1 : Molecular cytogenetic characterization by use of spectral karyotyping and comparative genomic hybridizationNISHIO, Jun; IWASAKI, Hiroshi; NABESHIMA, Kazuki et al.International journal of oncology. 2005, Vol 27, Num 2, pp 361-369, issn 1019-6439, 9 p.Article

Both IGH translocations and chromosome 13q deletions are early events in monoclonal gammopathy of undetermined significance and do not evolve during transition to multiple myelomaKAUFMANN, H; ACKERMANN, J; ZIELINSKI, C et al.Leukemia. 2004, Vol 18, Num 11, pp 1879-1882, issn 0887-6924, 4 p.Article

Molecular monitoring of response to imatinib (Glivec®) in CML patients pretreated with interferon alpha. Low levels of residual disease are associated with continuous remission : Spotlight on imatinib as a model for signal transduction inhibitorsPASCHKA, P; MÜLLER, M. C; GSCHAIDMEIER, H et al.Leukemia. 2003, Vol 17, Num 9, pp 1687-1694, issn 0887-6924, 8 p.Article