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American Journal of Medical Genetics. Part A|April 29, 2010
Molecular and clinical characterization of patients with overlapping 10p deletionsAnna Lindstrand, Helena Malmgren, Annapia Verri, et al.
European Journal of Human Genetics : EJHG|December 4, 2008
Breakpoint characterization of a novel approximately 59 kb genomic deletion on 19q13.42 in autosomal-dominant retinitis pigmentosa with incomplete penetranceLinda Köhn, Sara J Bowne, Lori S Sullivan, et al.
British Journal of Haematology|September 27, 2006
Characterisation of dic(9;20)(p11-13;q11) in childhood B-cell precursor acute lymphoblastic leukaemia by tiling resolution array-based comparative genomic hybridisation reveals clustered breakpoints at 9p13.2 and 20q11.2Jacqueline Schoumans, Bertil Johansson, Martin Corcoran, et al.
British Journal of Haematology|May 29, 2015
The clinical impact of IKZF1 deletions in paediatric B-cell precursor acute lymphoblastic leukaemia is independent of minimal residual disease stratification in Nordic Society for Paediatric Haematology and Oncology treatment protocols used between 1992 and 2013Linda Olsson, Ingegerd Ivanov Öfverholm, Ulrika Norén-Nyström, et al.
Cancers|December 18, 2019
The Genetic Architecture of Gliomagenesis-Genetic Risk Variants Linked to Specific Molecular SubtypesWendy Yi-Ying Wu, Gunnar Johansson, Carl Wibom, et al.
Genes, Chromosomes & Cancer|August 3, 2004
Spontaneously immortalized human T lymphocytes develop gain of chromosomal region 2p13-24 as an early and common genetic eventJan Konrad Siwicki, Mattias Berglund, Jolanta Rygier, et al.
Human Mutation|February 14, 2015
Mutations in collagen, type XVII, alpha 1 (COL17A1) cause epithelial recurrent erosion dystrophy (ERED)Frida Jonsson, Berit Byström, Alice E Davidson, et al.
Human Molecular Genetics|September 11, 2008
Alterations in the expression, structure and function of progesterone receptor membrane component-1 (PGRMC1) in premature ovarian failureMahmoud Reza Mansouri, Jens Schuster, Jitendra Badhai, et al.
Journal of Hematology & Oncology|April 15, 2014
Clinical and genetic features of pediatric acute lymphoblastic leukemia in Down syndrome in the Nordic countriesCatarina Lundin, Erik Forestier, Mette Klarskov Andersen, et al.
Genes, Chromosomes & Cancer|February 8, 2007
Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literatureErik Forestier, Mette K Andersen, Kirsi Autio, et al.
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