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Results: 1-9 |
Results: 9
SALVAGE OF PATIENTS WITH ACUTE PROMYELOCYTIC LEUKEMIA WITH RESIDUAL DISEASE FOLLOWING ABMT PERFORMED IN 2ND CR USING ALL-TRANS-RETINOIC ACID
Authors: GRIMWADE D JAMAL R GOULDEN N KEMPSKI H MASTRANGELO S VEYS P
Citation: D. Grimwade et al., SALVAGE OF PATIENTS WITH ACUTE PROMYELOCYTIC LEUKEMIA WITH RESIDUAL DISEASE FOLLOWING ABMT PERFORMED IN 2ND CR USING ALL-TRANS-RETINOIC ACID, British Journal of Haematology, 103(2), 1998, pp. 559-562
LOSS OF HETEROZYGOSITY, MICROSATELLITE INSTABILITY, AND GENETIC-VARIATION AT THE MLL LOCUS IN CHILDHOOD AND INFANT LEUKEMIA
Authors: WEBB JC GOLOVLEVA I SIMPKINS AH KEMPSKI H STURT N CHESSELLS JM BRICKELL PM
Citation: Jc. Webb et al., LOSS OF HETEROZYGOSITY, MICROSATELLITE INSTABILITY, AND GENETIC-VARIATION AT THE MLL LOCUS IN CHILDHOOD AND INFANT LEUKEMIA, British Journal of Haematology, 101, 1998, pp. 175-175
STRUCTURAL AND NUMERICAL ABNORMALITIES OF CHROMOSOME-21 IN PEDIATRIC LEUKEMIA
Authors: KEMPSKI H CHESSELLS J REEVES B
Citation: H. Kempski et al., STRUCTURAL AND NUMERICAL ABNORMALITIES OF CHROMOSOME-21 IN PEDIATRIC LEUKEMIA, Journal of Medical Genetics, 34, 1997, pp. 43-43
LOCALIZATION OF THE 8-13 TRANSLOCATION BREAKPOINT ASSOCIATED WITH MYELOPROLIFERATIVE DISEASE TO A 1.5 MBP REGION OF CHROMOSOME-13
Authors: KEMPSKI H MACDONALD D MICHALSKI AJ ROBERTS T GOLDMAN JM CROSS NCP COWELL JK
Citation: H. Kempski et al., LOCALIZATION OF THE 8-13 TRANSLOCATION BREAKPOINT ASSOCIATED WITH MYELOPROLIFERATIVE DISEASE TO A 1.5 MBP REGION OF CHROMOSOME-13, Genes, chromosomes & cancer, 12(4), 1995, pp. 283-287
A CASE OF ACUTE MEGAKARYOBLASTIC LEUKEMIA WITH T(X-6)(P11.21-Q23) HAVING AN X-CHROMOSOME BREAKPOINT WITHIN A 450-KB REGION WHICH IS ALSO DISRUPTED IN 2 CLASSES OF SOLID TUMORS
Authors: REEVES BR KNIGHT JC RENWICK PJ JANI K KEMPSKI H
Citation: Br. Reeves et al., A CASE OF ACUTE MEGAKARYOBLASTIC LEUKEMIA WITH T(X-6)(P11.21-Q23) HAVING AN X-CHROMOSOME BREAKPOINT WITHIN A 450-KB REGION WHICH IS ALSO DISRUPTED IN 2 CLASSES OF SOLID TUMORS, Leukemia, 9(4), 1995, pp. 723-725
2 CATEGORIES OF SYNOVIAL SARCOMA DEFINED BY DIVERGENT CHROMOSOME-TRANSLOCATION BREAKPOINTS IN XP11.2, WITH IMPLICATIONS FOR THE HISTOLOGIC SUB-CLASSIFICATION OF SYNOVIAL SARCOMA
Authors: RENWICK PJ REEVES BR DALCIN P FLETCHER CDM KEMPSKI H SCIOT R KAZMIERCZAK B JANI K SONOBE H KNIGHT JC
Citation: Pj. Renwick et al., 2 CATEGORIES OF SYNOVIAL SARCOMA DEFINED BY DIVERGENT CHROMOSOME-TRANSLOCATION BREAKPOINTS IN XP11.2, WITH IMPLICATIONS FOR THE HISTOLOGIC SUB-CLASSIFICATION OF SYNOVIAL SARCOMA, Cytogenetics and cell genetics, 70(1-2), 1995, pp. 58-63
A CASE OF ACUTE MONOCYTIC LEUKEMIA WITH T(1117) INVOLVING A REARRANGEMENT OF MLL-1 AND A REGION PROXIMAL TO THE RARA GENE
Authors: REEVES BR KEMPSKI H JANI K BORROW J HOWE K SOLOMON E KEARNEY L COTTER F
Citation: Br. Reeves et al., A CASE OF ACUTE MONOCYTIC LEUKEMIA WITH T(1117) INVOLVING A REARRANGEMENT OF MLL-1 AND A REGION PROXIMAL TO THE RARA GENE, Cancer genetics and cytogenetics, 74(1), 1994, pp. 50-53
ISOLATION AND CHARACTERIZATION OF A PANEL OF COSMIDS WHICH ALLOWS UNEQUIVOCAL IDENTIFICATION OF CHROMOSOME DELETIONS INVOLVING THE RB1 GENEUSING FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: COWELL JK JAJU R KEMPSKI H
Citation: Jk. Cowell et al., ISOLATION AND CHARACTERIZATION OF A PANEL OF COSMIDS WHICH ALLOWS UNEQUIVOCAL IDENTIFICATION OF CHROMOSOME DELETIONS INVOLVING THE RB1 GENEUSING FLUORESCENCE IN-SITU HYBRIDIZATION, Journal of Medical Genetics, 31(4), 1994, pp. 334-337
DETECTION OF SUBMICROSCOPIC CHROMOSOMAL DELETIONS IN ANIRIDIA PATIENTS USING FLUORESCENCE IN-SITU HYBRIDIZATION AND A PANEL OF COSMIDS COVERING THE WT1 GENE
Authors: KEMPSKI H COWELL JK
Citation: H. Kempski et Jk. Cowell, DETECTION OF SUBMICROSCOPIC CHROMOSOMAL DELETIONS IN ANIRIDIA PATIENTS USING FLUORESCENCE IN-SITU HYBRIDIZATION AND A PANEL OF COSMIDS COVERING THE WT1 GENE, International journal of oncology, 3(5), 1993, pp. 937-940
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