Authors:
KNUTSEN T
MICKLEY LA
RIED T
GREEN ED
DUMANOIR S
SCHROCK E
MACVILLE M
NING Y
ROBEY R
POLYMEROPOULOS M
TORRES R
FOJO T
Citation: T. Knutsen et al., CYTOGENETIC AND MOLECULAR CHARACTERIZATION OF RANDOM CHROMOSOMAL REARRANGEMENTS ACTIVATING THE DRUG-RESISTANCE GENE, MDR1 P-GLYCOPROTEIN, IN DRUG-SELECTED CELL-LINES AND PATIENTS WITH DRUG-REFRACTORY ALL/, Genes, chromosomes & cancer, 23(1), 1998, pp. 44-54
Authors:
HESELMEYER K
HELLSTROM AC
BLEGEN H
SCHROCK E
SILFVERSWARD C
SHAH K
AUER G
RIED T
Citation: K. Heselmeyer et al., PRIMARY-CARCINOMA OF THE FALLOPIAN-TUBE - COMPARATIVE GENOMIC HYBRIDIZATION REVEALS HIGH GENETIC INSTABILITY AND A SPECIFIC, RECURRING PATTERN OF CHROMOSOMAL-ABERRATIONS, International journal of gynecological pathology, 17(3), 1998, pp. 245-254
Authors:
PHELAN MC
BLACKBURN W
ROGERS RC
CRAWFORD EC
COOLEY NR
SCHROCK E
NING Y
RIED T
Citation: Mc. Phelan et al., FISH ANALYSIS OF A COMPLEX CHROMOSOME REARRANGEMENT INVOLVING 9 BREAKPOINTS ON CHROMOSOME-6, CHROMOSOME-12, CHROMOSOME-14 AND CHROMOSOME-16, Prenatal diagnosis, 18(11), 1998, pp. 1174-1180
Authors:
AGARWAL SK
SCHROCK E
KESTER MB
BURNS AL
HEFFESS CS
RIED T
MARX SJ
Citation: Sk. Agarwal et al., COMPARATIVE GENOMIC HYBRIDIZATION ANALYSIS OF HUMAN PARATHYROID TUMORS, Cancer genetics and cytogenetics, 106(1), 1998, pp. 30-36
Authors:
NING Y
LIANG JC
NAGARAJAN L
SCHROCK E
RIED T
Citation: Y. Ning et al., CHARACTERIZATION OF 5Q DELETIONS BY SUBTELOMERIC PROBES AND SPECTRAL KARYOTYPING, Cancer genetics and cytogenetics, 103(2), 1998, pp. 170-172
Authors:
CHESI M
BERGSAGEL PL
SHONUKAN OO
MARTELLI ML
BRENTS LA
CHEN T
SCHROCK E
RIED T
KUEHL VM
Citation: M. Chesi et al., FREQUENT DYSREGULATION OF THE C-MAF PROTOONCOGENE AT 16Q23 BY TRANSLOCATION TO AN IG LOCUS IN MULTIPLE-MYELOMA, Blood, 91(12), 1998, pp. 4457-4463
Authors:
CHESI M
NARDINI E
BRENTS LA
SCHROCK E
RIED T
KUEHL WM
BERGSAGEL PL
Citation: M. Chesi et al., FREQUENT TRANSLOCATION T(4-14)(P16.3-Q32.3) IN MULTIPLE-MYELOMA IS ASSOCIATED WITH INCREASED EXPRESSION AND ACTIVATING MUTATIONS OF FIBROBLAST GROWTH-FACTOR RECEPTOR-3, Nature genetics, 16(3), 1997, pp. 260-264
Authors:
VELDMAN T
VIGNON C
SCHROCK E
ROWLEY JD
RIED T
Citation: T. Veldman et al., HIDDEN CHROMOSOME-ABNORMALITIES IN HEMATOLOGICAL MALIGNANCIES DETECTED BY MULTICOLOR SPECTRAL KARYOTYPING, Nature genetics, 15(4), 1997, pp. 406-410
Authors:
HESELMEYER K
MACVILLE M
SCHROCK E
BLEGEN H
HELLSTROM AC
SHAH K
AUER G
RIED T
Citation: K. Heselmeyer et al., ADVANCED-STAGE CERVICAL CARCINOMAS ARE DEFINED BY A RECURRENT PATTERNOF CHROMOSOMAL-ABERRATIONS REVEALING HIGH GENETIC INSTABILITY AND A CONSISTENT GAIN OF CHROMOSOME ARM 3Q, Genes, chromosomes & cancer, 19(4), 1997, pp. 233-240
Authors:
MACVILLE M
VELDMAN T
PADILLANASH H
WANGSA D
OBRIEN P
SCHROCK E
RIED T
Citation: M. Macville et al., SPECTRAL KARYOTYPING, A 24-COLOR FISH TECHNIQUE FOR THE IDENTIFICATION OF CHROMOSOMAL REARRANGEMENTS, HISTOCHEM C, 108(4-5), 1997, pp. 299-305
Authors:
RIED T
LIYANAGE M
DUMANOIR S
HESELMEYER K
AUER G
MACVILLE M
SCHROCK E
Citation: T. Ried et al., TUMOR CYTOGENETICS REVISITED - COMPARATIVE GENOMIC HYBRIDIZATION AND SPECTRAL KARYOTYPING, Journal of molecular medicine, 75(11-12), 1997, pp. 801-814
Authors:
PACKENHAM JP
DUMANOIR S
SCHROCK E
RISINGER JI
DIXON D
DENZ DN
EVANS JAC
BERCHUCK A
BARRETT JC
DEVEREUX TR
RIED T
Citation: Jp. Packenham et al., ANALYSIS OF GENETIC ALTERATIONS IN UTERINE LEIOMYOMAS AND LEIOMYOSARCOMAS BY COMPARATIVE GENOMIC HYBRIDIZATION, Molecular carcinogenesis, 19(4), 1997, pp. 273-279
Authors:
SCHROCK E
VELDMAN T
PADILLANASH H
NING Y
SPURBECK J
JALAL S
SHAFFER LG
PAPENHAUSEN P
KOZMA C
PHELAN MC
KJELDSEN E
SCHONBERG SA
OBRIEN P
BIESECKER L
DUMANOIR S
RIED T
Citation: E. Schrock et al., SPECTRAL KARYOTYPING REFINES CYTOGENETIC DIAGNOSTICS OF CONSTITUTIONAL CHROMOSOMAL-ABNORMALITIES, Human genetics, 101(3), 1997, pp. 255-262
Citation: Oq. Haas et al., DECIPHERING COMPLEX KARYOTYPES OF HEMATOLOGIC NEOPLASMS WITH SPECTRALKARYOTYPING (SKY), Cytogenetics and cell genetics, 77(1-2), 1997, pp. 35-35
Authors:
MIESCHER GC
TAYLOR V
OLIVIERI G
MINDERMANN T
SCHROCK E
STECK AJ
Citation: Gc. Miescher et al., EXTENSIVE SPLICE VARIATION AND LOCALIZATION OF THE EHK-1 RECEPTOR TYROSINE KINASE IN ADULT HUMAN BRAIN AND GLIAL TUMORS, Molecular brain research, 46(1-2), 1997, pp. 17-24
Citation: Sh. Bigner et E. Schrock, MOLECULAR CYTOGENETICS OF BRAIN-TUMORS, Journal of neuropathology and experimental neurology, 56(11), 1997, pp. 1173-1181
Authors:
SCHWENDEL A
LANGRECK H
REICHEL M
SCHROCK E
RIED T
DIETEL M
PETERSEN I
Citation: A. Schwendel et al., PRIMARY SMALL-CELL LUNG CARCINOMAS AND THEIR METASTASES ARE CHARACTERIZED BY A RECURRENT PATTERN OF GENETIC ALTERATIONS, International journal of cancer, 74(1), 1997, pp. 86-93
Authors:
COLEMAN AE
SCHROCK E
WEAVER Z
DUMANOIR S
YANG FT
FERGUSONSMITH MA
RIED T
JANZ S
Citation: Ae. Coleman et al., PREVIOUSLY HIDDEN CHROMOSOME-ABERRATIONS IN T(12-15)-POSITIVE BALB C PLASMACYTOMAS UNCOVERED BY MULTICOLOR SPECTRAL KARYOTYPING/, Cancer research, 57(20), 1997, pp. 4585-4592
Authors:
HESELMEYER K
DUMANOIR S
BLEGEN H
FRIBERG B
SVENSSON C
SCHROCK E
VELDMAN T
SHAH K
AUER G
RIED T
Citation: K. Heselmeyer et al., A RECURRENT PATTERN OF CHROMOSOMAL-ABERRATIONS AND IMMUNOPHENOTYPIC APPEARANCE DEFINES ANAL SQUAMOUS-CELL CARCINOMAS, British Journal of Cancer, 76(10), 1997, pp. 1271-1278
Authors:
HAWKINS AL
SCHROCK E
RIED T
JAFFEE E
GRIFFIN CA
Citation: Al. Hawkins et al., ANALYSIS OF COMPLEX CHROMOSOME-ABNORMALITIES IN PANCREATIC-CANCER CELL-LINES BY MULTICOLOR SPECTRAL KARYOTYPING (SKY), American journal of human genetics, 61(4), 1997, pp. 366-366
Authors:
PADILLANASH HM
VELDMAN T
SCHROCK E
HAAS O
ROWLEY JD
RIED T
Citation: Hm. Padillanash et al., CHROMOSOMAL-ABNORMALITIES REVEALED BY SPECTRAL KARYOTYPING IN HEMATOLOGICAL MALIGNANCIES, American journal of human genetics, 61(4), 1997, pp. 418-418
Authors:
WOLF NG
ABDULKARIM FW
FARVER C
RIED T
SCHROCK E
DUMANOIR S
SCHWARTZ S
Citation: Ng. Wolf et al., ANALYSIS OF OVARIAN BORDERLINE TUMORS USING COMPARATIVE GENOMIC HYBRIDIZATION (CGH) AND FLUORESCENCE IN-SITU HYBRIDIZATION (FISH), American journal of human genetics, 61(4), 1997, pp. 489-489