Arjan Buijs

Arjan Buijs

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Arjan Buijs

Arjan Buijs

Publications by authors named "Arjan Buijs"

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20Publications

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A survey of undetected, clinically relevant chromosome abnormalities when replacing postnatal karyotyping by Whole Genome Sequencing.

Eur J Med Genet 2019 Sep 22;62(9):103543. Epub 2018 Sep 22.

Department of Genetics, University Medical Centre Utrecht, Utrecht University, Utrecht, P.O. Box 85090, 3508 AB, Utrecht, the Netherlands.

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http://dx.doi.org/10.1016/j.ejmg.2018.09.010DOI Listing
September 2019

Lymphoblastic lymphoma with a triple-hit profile: a rare but distinct and relevant entity.

Hum Pathol 2017 05 17;63:171-176. Epub 2016 Nov 17.

Department of Pathology, University Medical Center Utrecht, 3584, CX, Utrecht, the Netherlands.

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http://dx.doi.org/10.1016/j.humpath.2016.11.002DOI Listing
May 2017

A neonate with a unique non-Down syndrome transient proliferative megakaryoblastic disease.

Pediatr Blood Cancer 2017 03 26;64(3). Epub 2016 Sep 26.

Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.

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http://dx.doi.org/10.1002/pbc.26230DOI Listing
March 2017

Outcome of allogeneic transplantation in newly diagnosed and relapsed/refractory multiple myeloma: long-term follow-up in a single institution.

Eur J Haematol 2016 Nov 3;97(5):479-488. Epub 2016 May 3.

Department of Hematology, VU University Medical Center, Amsterdam, the Netherlands.

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http://dx.doi.org/10.1111/ejh.12758DOI Listing
November 2016

Sequential cancer mutations in cultured human intestinal stem cells.

Nature 2015 May 29;521(7550):43-7. Epub 2015 Apr 29.

1] Hubrecht Institute, Royal Netherlands Academy of Arts and Sciences (KNAW) and UMC Utrecht, 3584CT Utrecht, The Netherlands [2] Cancer Genomics Netherlands, UMC Utrecht, 3584CG Utrecht, The Netherlands.

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http://dx.doi.org/10.1038/nature14415DOI Listing
May 2015

A ZMYM2-FGFR1 8p11 myeloproliferative neoplasm with a novel nonsense RUNX1 mutation and tumor lysis upon imatinib treatment.

Cancer Genet 2013 Apr;206(4):140-4

Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.

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http://dx.doi.org/10.1016/j.cancergen.2013.04.001DOI Listing
April 2013

A girl with an atypical form of ataxia telangiectasia and an additional de novo 3.14 Mb microduplication in region 19q12.

Eur J Med Genet 2012 Jan 27;55(1):49-55. Epub 2011 Aug 27.

Institut für Humangenetik, Universitätsmedizin der Johannes Gutenberg-Universität Mainz, Mainz, Germany.

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http://dx.doi.org/10.1016/j.ejmg.2011.08.001DOI Listing
January 2012

Identification of chromosomal abnormalities relevant to prognosis in chronic lymphocytic leukemia using multiplex ligation-dependent probe amplification.

Cancer Genet Cytogenet 2009 Dec;195(2):97-104

Department of Human Genetics, Radboud University Nijmegen Medical Center, PO Box 9101, 6500 HB Nijmegen, The Netherlands.

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http://dx.doi.org/10.1016/j.cancergencyto.2009.06.020DOI Listing
December 2009

Cytogenetic aberrations in neuropathy associated with IgM monoclonal gammopathy.

J Neurol Sci 2007 Sep 1;260(1-2):124-31. Epub 2007 Jun 1.

Department of Neurology, the Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, The Netherlands.

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http://linkinghub.elsevier.com/retrieve/pii/S0022510X0700288
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http://dx.doi.org/10.1016/j.jns.2007.04.022DOI Listing
September 2007

A new subtype of MLL-SEPT2 fusion transcript in therapy-related acute myeloid leukemia with t(2;11)(q37;q23): a case report and literature review.

Cancer Genet Cytogenet 2007 Jul;176(1):72-5

Department of Medical Genetics, University Medical Center Utrecht, PO Box 85090, 3508 AB Utrecht, The Netherlands.

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http://dx.doi.org/10.1016/j.cancergencyto.2007.04.001DOI Listing
July 2007