Monitoring of engraftment and progression of acute lymphoblastic leukemia in individual NOD/SCID mice von Nijmeijer, Bart A, Mollevanger, Paul, van Zelderen-Bhola, Shama L, Kluin-Nelemans, Hanneke C, Willemze, Roel, Falkenburg, J.H.Frederik

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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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Multiple supernumerary ring chromosomes of different origin in a patient: A clinical report and review of the literature von Beverstock, Geoff C., Bezrookove, Vladimir, Mollevanger, Paul, van de Kamp, Jacques J.P., Pearson, Peter, Kouwenberg, Jan M., Rosenberg, Carla

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Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndrome von Horsthemke, B, Maat-Kievit, A, Sleegers, E, van den Ouweland, A, Buiting, K, Lich, C, Mollevanger, P, Beverstock, G, Gillessen-Kaesbach, G, Schwanitz, G

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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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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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Multiple supernumerary ring chromosomes of different origin in a patient: A clinical report and review of the literature von Beverstock, Geoff C., Bezrookove, Vladimir, Mollevanger, Paul, van de Kamp, Jacques J.P., Pearson, Peter, Kouwenberg, Jan M., Rosenberg, Carla

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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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Nasopharyngeal Teratoma and Mosaic Tetrasomy 1q Detected at Amniocentesis 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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Ring Chromosome 4 as the Sole Cytogenetic Anomaly in a Chondroblastoma: A Case Report and Review of the Literature von van Zelderen-Bhola, Shama L., Bovée, Judith V.M.G., Wessels, Hans W., Mollevanger, Paul, Nijhuis, Jeroen V., van Eendenburg, Jaap D.H., Taminiau, Anthonie H.M., Hogendoorn, Pancras C.W.

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A second case of hexasomy 8 in myelodysplastic syndrome von Beverstock, Geoffrey C., Wessels, Hans W., Mollebanger, Paul, den Ottolander, Gerard J., Gottlieb, David J.

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Ring Chromosome 4 as the Sole Cytogenetic Anomaly in a Chondroblastoma von van Zelderen-Bhola, Shama L., Bovée, Judith V.M.G., Wessels, Hans W., Mollevanger, Paul, Nijhuis, Jeroen V., van Eendenburg, Jaap D.H., Taminiau, Anthonie H.M., Hogendoorn, Pancras C.W.

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Cytogenetic and fluorescence in situ hybridisation (FISH) analysis of ocular melanoma von Beverstockl, Geoffrey C., de Jager, Martine, de Waard-Siebinga, Ite, Kool, Jeanette, Mollevanger, Paul, Wessels, Hans, Hoogendoorn, Ed

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A case of isodicentric 7p as sole abnormality in a patient with acute myeloid leukemia von Beverstock, Geoffrey C., de Meijer, Paul H.E.M., Huinink, Daan ten Bokkel, Pruijt, Johannes F.M., den Ottolander, Gerard J., Wessels, Hans W., Mollevanger, Paul

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Trisomy 13 and myelodysplastic syndrome von Beverstock, Geoffrey C., Ploem, Jan E., Wessels, Hans, Keur, Daan v.d., Mollevanger, Paul

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Conformational Changes of Yeast tRNAPhe as Monitored by 31P NMR von SALEMINK, Paul J. M., REIJERSE, Ed J., MOLLEVANGER, Leo C. P. J., HILBERS, Cornelis W.

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