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Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|February 27, 2004
Reverse painting highlights the origin of chromosome aberrationsElisabeth Blennow
Best Practice & Research. Clinical Obstetrics & Gynaecology|December 12, 2002
Prenatal diagnosis: molecular genetics and cytogeneticsThe-Hung Bui, Elisabeth Blennow, Magnus Nordenskjöld
Lakartidningen|October 5, 2002
[New analytic methods provide answers regarding chromosome aberrations in 1-2 days]The-Hung Bui, Elisabeth Blennow, Magnus Nordenskjöld
Fertility and Sterility|October 19, 2010
Hidden mosaicism for a structural chromosome rearrangement: a rare explanation for recurrent miscarriages and affected offspring?Katarina Haapaniemi Kouru, Helena Malmgren, Irene White, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
Molecular cytogenetic characterization of an insertional translocation, ins(6;7)(p25;q33q34): deletion/duplication of 7q33-34 and clinical correlationsH Malmgren, G Malm, S Sahlén, et al.
American Journal of Medical Genetics. Part A|August 21, 2007
Distal 3p deletion syndrome: detailed molecular cytogenetic and clinical characterization of three small distal deletions and reviewHelena Malmgren, Sigrid Sahlén, Katarina Wide, et al.
Haematologica|May 21, 2009
Overexpression of CD123 correlates with the hyperdiploid genotype in acute lymphoblastic leukemiaMiroslav Djokic, Elisabet Björklund, Elisabeth Blennow, et al.
European Journal of Haematology|April 16, 2002
Spectral karyotyping and interphase FISH reveal abnormalities not detected by conventional G-banding. Implications for treatment stratification of childhood acute lymphoblastic leukaemia: detailed analysis of 70 casesAnn Nordgren, Mats Heyman, Sigrid Sahlén, et al.
Molecular Human Reproduction|April 13, 2006
PGD for dystrophin gene deletions using fluorescence in situ hybridizationH Malmgren, I White, S Johansson, et al.
International Journal of Molecular Medicine|January 14, 2004
DNA copy-number analysis of the 22q11 deletion-syndrome region using array-CGH with genomic and PCR-based targetsKiran Kumar Mantripragada, Isabel Tapia-Páez, Elisabeth Blennow, et al.
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