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Anticancer Research|September 12, 2013
Immunological response after WT1 mRNA-loaded dendritic cell immunotherapy in ovarian carcinoma and carcinosarcomaAn Coosemans, Anke Vanderstraeten, Sandra Tuyaerts, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|July 8, 2011
Evolution in endometrial cancer: evidence from an immunohistochemical studyIngrid Vandenput, Jone Trovik, Karin Leunen, et al.
Human Molecular Genetics|June 19, 2003
CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behaviorSuzanna G M Frints, Peter Marynen, Dieter Hartmann, et al.
American Journal of Human Genetics|August 5, 2005
Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in malesHilde Van Esch, Marijke Bauters, Jaakko Ignatius, et al.
American Journal of Medical Genetics. Part A|April 14, 2009
Phenotype and 244k array-CGH characterization of chromosome 13q deletions: an update of the phenotypic map of 13q21.1-qterMaria Kirchhoff, Anne-Marie Bisgaard, Radka Stoeva, et al.
Anticancer Research|December 11, 2013
Wilms' Tumor Gene 1 (WT1)--loaded dendritic cell immunotherapy in patients with uterine tumors: a phase I/II clinical trialAn Coosemans, Anke Vanderstraeten, Sandra Tuyaerts, et al.
Nature Genetics|August 21, 2007
Germline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotypeHilde Brems, Magdalena Chmara, Mourad Sahbatou, et al.
American Journal of Human Genetics|December 17, 2009
Dosage-dependent severity of the phenotype in patients with mental retardation due to a recurrent copy-number gain at Xq28 mediated by an unusual recombinationJoke Vandewalle, Hilde Van Esch, Karen Govaerts, et al.
American Journal of Human Genetics|May 22, 2004
High prevalence of SLC6A8 deficiency in X-linked mental retardationEfraim H Rosenberg, Ligia S Almeida, Tjitske Kleefstra, et al.
Folia Medica|February 13, 2009
Clinical and molecular-cytogenetic studies of cryptic chromosome aberrations in individuals with idiopathic mental retardation and multiple congenital malformationsRadka E Stoeva, Liliana I Grozdanova, Joris R Vermeesch, et al.
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