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La ricerca find articoli where authors phrase all words ' BEVERSTOCK GC' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 33 riferimenti
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    1. Bezrookove, V; Hansson, K; van der Burg, M; van der Smagt, JJ; Hilhorst-Hofstee, Y; Wiegant, J; Beverstock, GC; Raap, AK; Tanke, H; Breuning, MH; Rosenberg, C
      Individuals with abnormal phenotype and normal G-banding karyotype: improvement and limitations in the diagnosis by the use of 24-colour FISH

      HUMAN GENETICS
    2. van der Smagt, JJ; Beverstock, GC; Breuning, MH; Kanhai, HHH; Vandenbussche, FPHA
      Assessment of prenatal karyotypes

      HUMAN REPRODUCTION
    3. van der Reijden, BA; Dauwerse, HG; Giles, RH; Jagmohan-Changur, S; Wijmenga, C; Liu, PP; Smit, B; Wessels, HW; Beverstock, GC; Jotterand-Bellomo, M; Martinet, D; Muhlematter, D; Lafage-Pochitaloff, M; Gabert, J; Reiffers, J; Bilhou-Nabera, C; van Ommen, GJB; Hagemeijer, A; Breuning, MH
      Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered

      ONCOGENE
    4. Beverstock, GC; Mollevanger, P; Baaij, M; Lind, J; van Ieperen, L; Bartelings, MM; Teunissen, K; Brandenburg, H; Van Opstal, D; Los, F
      Nasopharyngeal teratoma and mosaic tetrasomy 1q detected at amniocentesis - A case report and review of the literature

      CANCER GENETICS AND CYTOGENETICS
    5. OOSTERWIJK JC; MESKER WE; OUWERKERKVANVELZEN MCM; KNEPFLE CFHM; WIESMEIJER CC; BEVERSTOCK GC; VANOMMEN GJB; TANKE HJ; KANHAI HHH
      FETAL CELL DETECTION IN MATERNAL BLOOD - A MULTIPARAMETER STUDY IN 236 SAMPLES USING ERYTHROBLAST MORPHOLOGY, DAB AND HBF STAINING AND FISHANALYSIS

      European journal of human genetics
    6. BEVERSTOCK GC; HANSSON K; HELDERMANVANDENENDEN TJM; BROCKERVRIENDS A; KLUMPER F; BARTELINGS M; DOBBEVANMEERENDONK W; ROOSMALEN JV; KOLKMAN PH; KANHAI HHH
      A NEAR FALSE-NEGATIVE FINDING OF MOSAIC TRISOMY-21 - A CAUTIONARY TALE

      Prenatal diagnosis
    7. OOSTERWIJK JC; MESKER WE; OUWERKERKVANVELZEN MCM; KNEPFLE CFHM; WIESMEIJER KC; BEVERSTOCK GC; VANOMMEN GJB; TANKE HJ; KANHAI HHH
      PRENATAL-DIAGNOSIS OF TRISOMY-13 ON FETAL CELLS OBTAINED FROM MATERNAL BLOOD AFTER MINOR ENRICHMENT

      Prenatal diagnosis
    8. OOSTERWIJK JC; MESKER WE; OUWERKERKVANVELZEN MCM; KNEPFLE CFHM; WIESMEIJER KC; VANDENBURG MJM; BEVERSTOCK GC; BERNINI LF; VANOMMEN GJB; KANHAI HHH; TANKE HJ
      DEVELOPMENT OF A PREPARATION AND STAINING METHOD FOR FETAL ERYTHROBLASTS IN MATERNAL BLOOD - SIMULTANEOUS IMMUNOCYTOCHEMICAL STAINING AND FISH ANALYSIS

      Cytometry
    9. OOSTERWIJK JC; MESKER WE; OUWERKERKVANVELZEN MCM; KNEPFLE CFHM; WIESMEIJER KC; BEVERSTOCK GC; VANOMMEN GJB; KANHAI HHH; TANKE HJ
      FETAL CELL DETECTION IN MATERNAL BLOOD - A STUDY IN 236 SAMPLES USINGERYTHROBLAST MORPHOLOGY, DAB AND HBF STAINING, AND FISH ANALYSIS

      Cytometry
    10. KROEF MJPL; BOLK MJW; MUUS P; WESSELS JW; BEVERSTOCK GC; WILLEMZE R; LANDEGENT JE
      MOSAICISM OF THE 5Q DELETION AS ASSESSED BY INTERPHASE FISH IS A COMMON PHENOMENON IN MDS AND RESTRICTED TO MYELOID CELLS

      Leukemia
    11. GILES RH; DAUWERSE JG; HIGGINS C; PETRIJ F; WESSELS JW; BEVERSTOCK GC; DOHNER H; JOTTERANDBELLOMO M; FALKENBURG JHF; SLATER RM; VANOMMEN GJB; HAGEMEIJER A; VANDERREIJDEN BA; BREUNING MH
      DETECTION OF CBP REARRANGEMENTS IN ACUTE MYELOGENOUS LEUKEMIA WITH T(8-16)

      Leukemia
    12. BEVERSTOCK GC; HELDERMAN A; KLUMPER F; BARTELINGS M; VANROOSMALEN J; KOLKMAN PH; KANHAI HHH
      A NEAR FALSE-NEGATIVE FINDING OF MOSAIC TRISOMY-21 - A CAUTIONARY TALE

      Cytogenetics and cell genetics
    13. BEVERSTOCK GC; KLUMPER F; VANDERENDEN ATJMH
      YET ANOTHER VARIATION ON THE THEME OF CHROMOSOME-18 HETEROMORPHISMS

      Prenatal diagnosis
    14. VANZELDERENBHOLA SL; BRESLAUSIDERIUS EJ; BEVERSTOCK GC; STOLTEDIJKSTRA I; DEVRIES LS; DEPATER JM
      PRENATAL AND POSTNATAL INVESTIGATION OF A CASE WITH MILLER-DIEKER SYNDROME DUE TO A FAMILIAL CRYPTIC TRANSLOCATION T(17-20) (P13.3-Q13.3) DETECTED BY FLUORESCENCE IN-SITU HYBRIDIZATION

      Prenatal diagnosis
    15. BEVERSTOCK GC; WESSELS HW; MOLLEVANGER P; DENOTTOLANDER GJ; GOTTLIEB DJ
      A 2ND CASE OF HEXASOMY-8 IN MYELODYSPLASTIC SYNDROME

      Cancer genetics and cytogenetics
    16. KANT SG; VANHAERINGEN A; BAKKER E; STEC I; DONNAI D; MOLLEVANGER P; BEVERSTOCK GC; LINDEMANKUSSE MC; VANOMMEN GJB
      PITT-ROGERS-DANKS-SYNDROME AND WOLF-HIRSCHHORN-SYNDROME ARE CAUSED BYA DELETION IN THE SAME REGION ON CHROMOSOME 4P16.3

      Journal of Medical Genetics
    17. VANDERREIJDEN BA; MARTINET D; DAUWERSE JG; GILES RH; WESSELS JW; BEVERSTOCK GC; SMIT B; MUHLEMATTER D; BELLOMO MJ; GABERT J; LAFAGEPOCHITALOFF M; REIFFERS J; BILHOUNABERA C; VANOMMEN GJB; HAGEMEIJER A; BREUNING MH
      SIMPLE METHOD FOR DETECTION OF MYH11 DNA REARRANGEMENTS IN PATIENTS WITH INV(16)(P13Q22) AND ACUTE MYELOID-LEUKEMIA

      Leukemia
    18. OOSTERWIJK JC; MESKER WE; OUWERKERK MCM; KNEPFLE CFHM; VANDERBURG MJM; WIESMEIJER CC; BEVERSTOCK GC; LOSEKOOT M; BERNINI LF; VANOMMEN GJB; VANDEKAMP JJP; KANHAI HHH; TANKE HJ
      DETECTION OF FETAL ERYTHROBLASTS IN MATERNAL BLOOD BY ONESTEP GRADIENT ENRICHMENT AND IMMUNOCYTOCHEMICAL RECOGNITION

      Early human development
    19. GILES RH; PETRIJ F; DAUWERSE JG; BEVERSTOCK GC; HAGEMEIJER A; PETERS DJM; BREUNING MH
      CONSTRUCTION OF A 850-KB COSMID CONTIG SURROUNDING THE CBP GENE, INVOLVED IN RUBINSTEIN-TAYBI SYNDROME AND ANLL M4 M5 WITH T(8-16)(P11-P13.3)/

      Cytogenetics and cell genetics
    20. BEVERSTOCK GC; DEMEIJER PHEM; HUININK DT; PRUIJT JFM; DENOTTOLANDER GJ; WESSELS HW; MOLLEVANGER P
      A CASE OF ISODICENTRIC 7P AS SOLE ABNORMALITY IN A PATIENT WITH ACUTEMYELOID-LEUKEMIA

      Cancer genetics and cytogenetics
    21. VANDERLUIJT RB; TOPS CMJ; KHAN PM; VANDERKLIFT HM; BREUKEL C; VANLEEUWENCORNELISSE ISJ; DAUWERSE HG; BEVERSTOCK GC; VANNOORT E; SNEL P; SLORS FJM; VASEN HFA; FODDE R
      MOLECULAR, CYTOGENETIC, AND PHENOTYPIC STUDIES OF A CONSTITUTIONAL RECIPROCAL TRANSLOCATION T(5-10)(Q22-Q25) RESPONSIBLE FOR FAMILIAL ADENOMATOUS POLYPOSIS IN A DUTCH PEDIGREE

      Genes, chromosomes & cancer
    22. ARTS WFM; HOFSTEE Y; DREJER GF; BEVERSTOCK GC; OOSTERWIJK JC
      CEREBELLAR AND BRAIN-STEM HYPOPLASIA IN A CHILD WITH A PARTIAL MONOSOMY FOR THE SHORT ARM OF CHROMOSOME-5 AND PARTIAL TRISOMY FOR THE SHORTARM OF CHROMOSOME-10

      Neuropediatrics
    23. GILES RH; PETRIJ F; DAUWERSE JG; VANDERREIJDEN BA; BEVERSTOCK GC; HAGEMEIJER A; BREUNING MH
      THE TRANSLOCATION T(8-16) IN ANLL M4 M5 DISRUPTS THE CBP GENE ON CHROMOSOME-16/

      Blood
    24. COIGNET LJA; SCHUURING E; KIBBELAAR RE; RAAP AK; KLEIVERDA JK; BERTHEAS MF; WIEGANT J; BEVERSTOCK GC; KLUIN PM
      DELETION OF 11Q13 REARRANGEMENTS IN HEMATOLOGIC MALIGNANCIES BY DOUBLE COLOR FLUORESCENCE IN-SITU HYBRIDIZATION

      Blood
    25. HAAK HL; WIJERMANS PW; VONWEERT J; BEVERSTOCK GC
      CYTOGENETIC ANALYSIS OF MULTIPLE-MYELOMA

      Blood
    26. VANDERREIJDEN BA; LOMBARDO M; DAUWERSE HG; GILES RH; MUHLEMATTER D; BELLOMO MJ; WESSELS HW; BEVERSTOCK GC; VANOMMEN GJB; HAGEMEIJER A; BREUNING MH
      RT-PCR DIAGNOSIS OF PATIENTS WITH ACUTE NONLYMPHOCYTIC LEUKEMIA AND INV(16)(P13Q22) AND IDENTIFICATION OF NEW ALTERNATIVE SPLICING IN CBFB-MYH11 TRANSCRIPTS

      Blood
    27. KLUINNELEMANS HC; BEVERSTOCK GC; MOLLEVANGER P; WESSELS HW; HOOGENDOORN E; WILLEMZE R; FALKENBURG JHF
      PROLIFERATION AND CYTOGENETIC ANALYSIS OF HAIRY-CELL LEUKEMIA UPON STIMULATION VIA THE CD40 ANTIGEN

      Blood
    28. KLUINNELEMANS HC; BEVERSTOCK GC; MOLLEVANGER P; WESSELS HW; HOOGENDOORN E; WILLEMZE R; FALKENBURG JHF
      PROLIFERATION AND CYTOGENETIC ANALYSIS OF HAIRY-CELL LEUKEMIA UPON STIMULATION VIA THE CD40 ANTIGEN

      Blood
    29. DAUWERSE JG; WESSELS JW; GILES RH; WIEGANT J; VANDERREIJDEN BA; FUGAZZA G; JUMELET EA; SMIT E; BAAS F; RAAP AK; HAGEMEIJER A; BEVERSTOCK GC; VANOMMEN GJB; BREUNING MH
      CLONING THE BREAKPOINT CLUSTER REGION OF THE INV(16) IN ACUTE NONLYMPHOCYTIC LEUKEMIA M4 EO

      Human molecular genetics
    30. LEWIS JP; TANKE HJ; RAAP AK; BEVERSTOCK GC; KLUINNELEMANS HC
      SOMATIC PAIRING OF CENTROMERES AND SHORT ARMS OF CHROMOSOME-15 IN THEHEMATOPOIETIC AND LYMPHOID SYSTEM

      Human genetics
    31. KIBBELAAR RE; MULDER JWR; DREEF EJ; VANKAMP H; FIBBE WE; WESSELS JW; BEVERSTOCK GC; HAAK HL; KLUIN PM
      DETECTION OF MONOSOMY-7 AND TRISOMY-8 IN MYELOID NEOPLASIA - A COMPARISON OF BANDING AND FLUORESCENCE IN-SITU HYBRIDIZATION

      Blood
    32. VANDERREIJDEN BA; DAUWERSE JG; WESSELS JW; BEVERSTOCK GC; HAGEMEIJER A; VANOMMEN GJB; BREUNING MH
      A GENE FOR A MYOSIN PEPTIDE IS DISRUPTED BY THE INV(16)(P13Q22) IN ACUTE NONLYMPHOCYTIC LEUKEMIA M4EO

      Blood
    33. KIBBELAAR RE; VANKAMP H; DREEF EJ; DEGROOTSWINGS G; KLUINNELEMANS JC; BEVERSTOCK GC; FIBBE WE; KLUIN PM
      COMBINED IMMUNOPHENOTYPING AND DNA INSITU HYBRIDIZATION TO STUDY LINEAGE INVOLVEMENT IN PATIENTS WITH MYELODYSPLASTIC SYNDROMES

      Blood


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Documento generato il 16/01/21 alle ore 11:26:06