LAF4, an AF4-related gene, is fused to MLL in infant acute lymphoblastic leukemia von von Bergh, Anne R.M., Beverloo, H. Berna, Rombout, Paul, van Wering, Elisabeth R., van Weel, Margreet H., Beverstock, Geoffrey C., Kluin, Philip M., Slater, Rosalyn M., Schuuring, Ed

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Prenatal diagnosis of trisomy 13 on fetal cells obtained from maternal blood after minor enrichment von Oosterwijk, Jan C., Mesker, Wilma E., Ouwerkerk-Van Velzen, Maria C. M., Knepflé, Cecile F. H. M., Wiesmeijer, Karien C., Beverstock, Geoffrey C., Van Ommen, Gert-Jan B., Tanke, Hans J., Kanhai, Humphrey H. H.

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Effect of Mast Cell Growth Factor (c-kit ligand) on Clonogenic Leukemic Precursor Cells von Henriëtte, M.Goselink, Douglas, E. Williams, Willem, E. Fibbe, Hans, W. Wessels, Geoffrey, C. Beverstock, Roel, Willemze, Frederik, J.H. Falkenburg

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A novel t(6;14)(q25∼q27;q32) in acute myelocytic leukemia involves the BCL11B gene von Bezrookove, Vladimir, van Zelderen-Bhola, Shama L., Brink, Antoinette, Szuhai, Károly, Raap, Anton K., Barge, Renee, Beverstock, Geoffrey C., Rosenberg, Carla

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Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3 von BREUNING, M. H, DAUWERSE, H. G, VAN DEN BOOGAARD, M.-J, DE PATER, J. M, MARIMAN, E. C. M, HAMEL, B. C. J, HIMMELBAUER, H, FRISCHAUF, A.-M, STALLINGS, R. L, HAMEL, B. C. J, HIMMELBAUER, H, FUGAZZA, G, BEVERSTOCK, G. C, VAN OMMEN, G.-J. B, HENNEKAM, R. C. M, SARIS, J. J, SPRUIT, L, WIJNEN, H, TOMMERUP, N, VAN DER HAGEN, C. B, IMAIZUMI, K, KUROKI, Y

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Proliferation and Cytogenetic Analysis of Hairy Cell Leukemia Upon Stimulation Via the CD40 Antigen von Kluin-Nelemans, Hanneke C., Beverstock, Geoffrey C., Mollevanger, Paul, Wessels, Hans W., Hoogendoorn, Ed, Willemze, Roel, Falkenburg, J.H.Frederik

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LETTER TO THE EDITOR. YET ANOTHER VARIATION ON THE THEME OF CHROMOSOME 18 HETERMORPHISMS? von BEVERSTOCK, GEOFFREY C., KLUMPER, FRANS, HELDERMAN-V. D. ENDEN, APOLLONIA T. J.

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Nasopharyngeal Teratoma and Mosaic Tetrasomy 1q Detected at Amniocentesis: A Case Report and Review of the Literature von Beverstock, Geoffrey C, Mollevanger, Paul, Baaij, Marjolein, Lind, J, van Ieperen, Liesbeth, Bartelings, Margot M, Teunissen, Katinka, Brandenburg, Helen, Van Opstal, Diane, Los, Frans

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Pitt-Rogers-Danks syndrome and Wolf-Hirschhorn syndrome are caused by a deletion in the same region on chromosome 4p16.3 von KANT, S. G, VAN HAERINGEN, A, BAKKER, E, STEC, I, DONNAI, D, MOLLEVANGER, P, BEVERSTOCK, G. C, LINDEMAN-KUSSE, M. C, VAN OMMEN, G.-J. B

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Somatic pairing of centromeres and short arms of chromosome 15 in the hematopoietic and lymphoid system von LEWIS, J. P, TANKE, H. J, RAAP, A. K, BEVERSTOCK, G. C, KLUIN-NELEMANS, H. C

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Premature menopause because of an inherited deletion in the long arm of the X-chromosome von Veneman, Thiemo F., Beverstock, Geoffrey C., Exalto, Niek, Mollevanger, Paul

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Molecular, cytogenetic, and phenotypic studies of a constitutional reciprocal translocation t(5; I0)(q22; q25) responsible for familial adenomatous polyposis in a Dutch pedigree von Van Der Luijt, Rob B., Tops, Carli M. J., Khan, P. Meera, Van Der Klift, Heleen M., Breukel, Cor, Van Leeuwen-Cornelisse, Inge S. J., Dauwerse, Hans G., Beverstock, Geoffrey C., Van Noort, Ellen, Snel, Pleun, Slors, Frederik J. M., Vasen, Hans F. A., Fodde, Riccardo

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Sequential development of peripheral T‐cell lymphoma in the course of chronic myelogenous leukemia von Blonk, Marion C., van der Valk, Paul, Beverstock, Geoffrey C., Ossenkoppele, Gerrit J.

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Nonradioactive in situ hybridisation of the translocation t(1;7) in myeloid malignancies von Kibbelaar, Robert E., Mulder, Jan-Willem R., Dreef, Enno J., Kluin, Philip M., Kamp, Harmen Van, Haak, Hans L., Raap, Anton K., Wessels, Hans W., Beverstock, Geoffrey C.

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Fetal blood group determination in first-trimester pregnancy for the management of severe immunization von Kanhai, Humphrey H., Gravenhorst, Jack Bennebroek, Gemke, Reinoud J., Overbeeke, Marijke A., Bernini, Luigi F., Beverstock, Geoffrey C.

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T‐cell prolymphocytic leukemia with an unusual phenotype CD4+ CD8 von Kluin‐Nelemans, Hanneke C., Gmelig‐Meyling, Frits H. J., Kootte, Antoinette M. M., Den Ottolander, Gerard J., Termijtelen, Annemarie, Kluin, Philip M., Beverstock, Geoffrey C., Brand, Anneke

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Characterization of a New Human B Cell Line (Bonna-12) with Trisomy 9 and Trisomy 12 Chromosomal Abnormality von Wientjens, Gert-Jan H. M., Jansen, Joop H., Wessels, Hans W., Kibbelaar, Robert E., Beverstock, Geoffrey C., Brederoo, Pieter, Kluin-nelemans, Hanneke C.

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der(1)t(1;9): A specific chromosome abnormality in polycythemia vera? von den Nijs van Weert, Jose I., Beverstock, Geoffrey C., Kievits, Tim, Haak, Hans L., Havik-Bogaard, Felicia C.T., Leeksma, Christiaan H.W.

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Fetal cell detection in maternal blood: A study in 236 samples using erythroblast morphology, DAB and Hbf staining, and FISH analysis von Oosterwijk, Jan C., Mesker, Wilma E., Ouwerkerk‐van Velzen, Maria C. M., Knepflé, Cecile F. H. M., Wiesmeijer, Karien C., Beverstock, Geoffrey C., van Ommen, Gert‐Jan B., Kanhai, Humphrey H. H., Tanke, Hans J.

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Development of a preparation and staining method for fetal erythroblasts in maternal blood: Simultaneous immunocytochemical staining and FISH analysis von Oosterwijk, Jan C., Mesker, Wilma E., Ouwerkerk‐van Velzen, Maria C. M., Knepflé, Cecile F. H. M., Wiesmeijer, Karien C., van den Burg, Marja J. M., Beverstock, Geoffrey C., Bernini, Luigi F., van Ommen, Gert‐Jan B., Kanhai, Humphrey H. H., Tanke, Hans J.

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