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The Journal of Pathology|February 1, 2005
Lack of Bcl-2 expression in follicular lymphoma may be caused by mutations in the BCL2 gene or by absence of the t(14;18) translocationMargit Schraders, Daphne de Jong, Philip Kluin, et al.
Journal of Human Genetics|October 10, 2014
A canonical splice site mutation in GIPC3 causes sensorineural hearing loss in a large Pakistani familySaima Siddiqi, Muhammad Ismail, Jaap Oostrik, et al.
Journal of Human Genetics|November 1, 2013
Novel mutation in AAA domain of BCS1L causing Bjornstad syndromeSaima Siddiqi, Saadat Siddiq, Atika Mansoor, et al.
The Annals of Otology, Rhinology, and Laryngology|May 19, 2011
Audioprofile-directed successful mutation analysis in a DFNA2/KCNQ4 (p.Leu274His) familyAnne-Martine R de Heer, Margit Schraders, Jaap Oostrik, et al.
British Journal of Haematology|August 14, 2008
Integrated genomic and expression profiling in mantle cell lymphoma: identification of gene-dosage regulated candidate genesMargit Schraders, Pedro Jares, Silvia Bea, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|January 13, 2009
Hypermutation in mantle cell lymphoma does not indicate a clinical or biological subentityMargit Schraders, Sabine Oeschger, Philip M Kluin, et al.
Genes, Chromosomes & Cancer|July 11, 2006
Quantitative microsatellite analysis to delineate the commonly deleted region 1p22.3 in mantle cell lymphomasAsha Balakrishnan, Nils von Neuhoff, Cornelia Rudolph, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|January 27, 2005
Increased vascularization predicts favorable outcome in follicular lymphomaAd Koster, Joannes H J M van Krieken, Marius A Mackenzie, et al.
Audiology & Neuro-Otology|January 22, 2011
Progressive sensorineural hearing loss and normal vestibular function in a Dutch DFNB7/11 family with a novel mutation in TMC1Anne-Martine R de Heer, Rob W J Collin, Patrick L M Huygen, et al.
Cancer Genetics and Cytogenetics|April 25, 2009
High-resolution genomic profiling of pediatric lymphoblastic lymphomas reveals subtle differences with pediatric acute lymphoblastic leukemias in the B-lineageMargit Schraders, Simon V van Reijmersdal, Eveline J Kamping, et al.
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