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BMJ (Clinical Research Ed.)|June 6, 1998
Screening for human T cell leukaemia/lymphoma virus among blood donors in Sweden: cost effectiveness analysisE Tynell, S Andersson, E Lithander, et al.
European Journal of Medical Genetics|January 16, 2007
A 6Mb deletion in band 2q22 due to a complex chromosome rearrangement associated with severe psychomotor retardation, microcephaly and distinctive dysmorphic facial featuresM J V Hoffer, Y Hilhorst-Hofstee, J Knijnenburg, et al.
Epidemiology and Infection|April 21, 2007
An outbreak of Escherichia coli O157:H7 infection in southern Sweden associated with consumption of fermented sausage; aspects of sausage production that increase the risk of contaminationL Sartz, B De Jong, M Hjertqvist, et al.
International Journal of Systematic and Evolutionary Microbiology|June 11, 2002
Polyphasic identification of Bacillus and Brevibacillus strains from clinical, dairy and industrial specimens and proposal of Brevibacillus invocatus sp. novN A Logan, G Forsyth, L Lebbe, et al.
Journal of Chemical Ecology|November 22, 2013
Identification and bioassay of sex pheromone components of carob moth,Ectomyelois ceratoniae (Zeller)T C Baker, W Francke, J G Millar, et al.
Hernia : the Journal of Hernias and Abdominal Wall Surgery|October 2, 2013
European Hernia Society classification of parastomal herniasM Śmietański, M Szczepkowski, J A Alexandre, et al.
Neurology|September 6, 2007
Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHDJ C de Greef, M Wohlgemuth, O A Chan, et al.
AJNR. American Journal of Neuroradiology|March 23, 2006
Cerebral white matter abnormalities in 6p25 deletion syndromeM S van der Knaap, M Kriek, W C G Overweg-Plandsoen, et al.
European Journal of Medical Genetics|June 14, 2011
Three new cases with a mosaicism involving a normal cell line and a cryptic unbalanced autosomal reciprocal translocationAntoinet C J Gijsbers, Johannes G Dauwerse, Cathy A J Bosch, et al.
American Journal of Medical Genetics. Part A|April 23, 2015
Clinical and molecular characterization of an infant with a tandem duplication and deletion of 19p13Ratna N G B Tan, Ruben S G M Witlox, Yvonne Hilhorst-Hofstee, et al.
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