Aberrant marker expression patterns on the CD34+CD38− stem cell compartment in acute myeloid leukemia allows to distinguish the malignant from the normal stem cell compartment both at diagnosis and in remission
VAN RHENEN, A, MOSHAVER, B, KELDER, A, FELLER, N, NIEUWINT, A. W. M, ZWEEGMAN, S, OSSENKOPPELE, G. J, SCHUURHUIS, G. J
Published in Leukemia (01.08.2007)
Published in Leukemia (01.08.2007)
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Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genes
Menko, FH, Kneepkens, CMF, De Leeuw, N, Peeters, EAJ, Van Maldergem, L, Kamsteeg, EJ, Davidson, R, Rozendaal, L, Lasham, CA, Peeters-Scholte, CMP, Jansweijer, MC, Hilhorst-Hofstee, Y, Gille, JJP, Heins, YM, Nieuwint, AWM, Sistermans, EA
Published in Clinical genetics (01.08.2008)
Published in Clinical genetics (01.08.2008)
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Familial Kleefstra syndrome due to maternal somatic mosaicism for interstitial 9q34.3 microdeletions
Willemsen, MH, Beunders, G, Callaghan, M, de Leeuw, N, Nillesen, WM, Yntema, HG, van Hagen, JM, Nieuwint, AWM, Morrison, N, Keijzers-Vloet, STM, Hoischen, A, Brunner, HG, Tolmie, J, Kleefstra, T
Published in Clinical genetics (01.07.2011)
Published in Clinical genetics (01.07.2011)
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Atypical progeroid syndrome: An unknown helicase gene defect?
Ruijs, M.W.G., van Andel, R.N.J., Oshima, J., Madan, K., Nieuwint, A.W.M., Aalfs, C.M.
Published in American journal of medical genetics. Part A (30.01.2003)
Published in American journal of medical genetics. Part A (30.01.2003)
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Mobilisation of haemopoietic progenitors in CML : a second course of intensive chemotherapy does not improve Ph-negativity in stem cell harvests
JANSSEN, J. J. W. M, VAN RIJN, R. S, NIEUWINT, A. W. M, CORNELISSEN, J. J, VAN DER HOLT, B, SCHUURHUIS, G.-J, VELLENGA, E, VERHOEF, G. E. G, OSSENKOPPELE, G. J, VAN DEN BERG, E, HAGEMEIJER, A, SLÄTER, R
Published in Bone marrow transplantation (Basingstoke) (01.06.2000)
Published in Bone marrow transplantation (Basingstoke) (01.06.2000)
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A triplication of the Williams–Beuren syndrome region in a patient with mental retardation, a severe expressive language delay, behavioural problems and dysmorphisms
Beunders, Gea, van de Kamp, Jiddeke M, Veenhoven, Reinier H, van Hagen, Johanna M, Nieuwint, Aggie W M, Sistermans, Erik A
Published in Journal of medical genetics (01.04.2010)
Published in Journal of medical genetics (01.04.2010)
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Interstitial deletion in 3q in a patient with blepharophimosis‐ptosis‐epicanthus inversus syndrome (BPES) and microcephaly, mild mental retardation and growth delay: Clinical report and review of the literature
de Ru, M.H., Gille, J.J.P., Nieuwint, A.W.M., Bijlsma, J.B., van der Blij, J.F., van Hagen, J.M.
Published in American journal of medical genetics. Part A (15.08.2005)
Published in American journal of medical genetics. Part A (15.08.2005)
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Non-P-glycoprotein mediated mechanism for multidrug resistance precedes P-glycoprotein expression during in vitro selection for doxorubicin resistance in a human lung cancer cell line
Baas, F, Jongsma, A P, Broxterman, H J, Arceci, R J, Housman, D, Scheffer, G L, Riethorst, A, van Groenigen, M, Nieuwint, A W, Joenje, H
Published in Cancer research (Chicago, Ill.) (01.09.1990)
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Published in Cancer research (Chicago, Ill.) (01.09.1990)
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Rapid detection of microdeletions using fluorescence in situ hybridisation (FISH) on buccal smears
NIEUWINT, A W M, VAN HAGEN, J M, HEINS, Y M, MADAN, K, TEN KATE, L P
Published in Journal of medical genetics (01.06.2000)
Published in Journal of medical genetics (01.06.2000)
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Genetic Transfer of Non-P-Glycoprotein-Mediated Multidrug Resistance (MDR) in Somatic Cell Fusion: Dissection of a Compound MDR Phenotype
Elisabeth W. H. M. Eijdems, Borst, Piet, Ans P. M. Jongsma, de Jong, Steven, Elisabeth G. E. de Vries, van Groenigen, Marjon, Carolina H. M. Versantvoort, Aggie W. M. Nieuwint, Baas, Frank
Published in Proceedings of the National Academy of Sciences - PNAS (15.04.1992)
Published in Proceedings of the National Academy of Sciences - PNAS (15.04.1992)
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First trimester diagnosis of cyclopia and holoprosencephaly
van Zalen-Sprock, R, van Vugt, J M, van der Harten, H J, Nieuwint, A W, van Geijn, H P
Published in Journal of ultrasound in medicine (01.08.1995)
Published in Journal of ultrasound in medicine (01.08.1995)
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DNA damage by chemically generated singlet oxygen
Lafleur, M V, Nieuwint, A W, Aubry, J M, Kortbeek, H, Arwert, F, Joenje, H
Published in Free radical research communications (1987)
Published in Free radical research communications (1987)
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Kabuki syndrome in son and low grade mosaic 45,X/46,XX in mother
Van Hagen, J M, Kwee, M L, Madan, K, Nieuwint, A W, Pals, G, ten Kate, L P
Published in Genetic counseling (1996)
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Published in Genetic counseling (1996)
Journal Article
Oxygen toxicity and chromosomal breakage in ataxia telangiectasia
Joenje, H, Nieuwint, A W, Taylor, A M, Harnden, D G
Published in Carcinogenesis (New York) (01.02.1987)
Published in Carcinogenesis (New York) (01.02.1987)
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Cytogenetic toxicity of paraquat and streptonigrin in Fanconi's anemia
Joenje, Hans, Nieuwint, Aggie W.M., Oostra, Anneke B., Arwert, Fré, de Koning, Han, Roozendaal, Klaas J.
Published in Cancer genetics and cytogenetics (01.03.1987)
Published in Cancer genetics and cytogenetics (01.03.1987)
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