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The New England Journal of Medicine|February 18, 1993
Direct diagnosis of myotonic dystrophy with a disease-specific DNA markerP Shelbourne, J Davies, J Buxton, et al.Prenatal Diagnosis|September 18, 2001
Clinical outcome of treatment cycles using preimplantation genetic diagnosis for structural chromosomal abnormalitiesM Fridström, L Ahrlund-Richter, E Iwarsson, et al.The Hematology Journal : the Official Journal of the European Haematology Association|March 29, 2002
Detailed characterization of a complex karyotype in a patient with primary plasma cell leukaemia using multicolour spectral karyotyping and micro-FISHA Nordgren, F Farnebo, M Björkholm, et al.Prenatal Diagnosis|February 17, 2001
Highly abnormal cleavage divisions in preimplantation embryos from translocation carriersE Iwarsson, H Malmgren, J Inzunza, et al.Molecular Human Reproduction|May 8, 2002
Single cell CGH analysis reveals a high degree of mosaicism in human embryos from patients with balanced structural chromosome aberrationsH Malmgren, S Sahlén, J Inzunza, et al.Prenatal Diagnosis|February 9, 1999
Application of single-needle blastomere biopsy in human preimplantation genetic diagnosisJ Inzunza, E Iwarsson, M Fridström, et al.Genes, Chromosomes & Cancer|April 2, 1998
Bilateral multiple renal oncocytomas and cysts associated with a constitutional translocation (8;9)(q24.1;q34.3) and a rare constitutional VHL missense substitutionB T Teh, E Blennow, S Giraud, et al.Journal of Cellular Biochemistry|April 20, 2006
In vitro culture conditions favoring selection of chromosomal abnormalities in human ES cellsM P Imreh, K Gertow, J Cedervall, et al.European Archives of Psychiatry and Clinical Neuroscience|January 1, 1997
Further studies on a male monozygotic triplet with schizophrenia: cytogenetical and neurobiological assessments in the patients and their parentsE G Jönsson, C Härnryd, T Johannesson, et al.Human Genetics|October 6, 1998
Characterization of the human synaptogyrin gene familyD Kedra, H Q Pan, E Seroussi, et al.Pageof 6