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American Journal of Medical Genetics|January 2, 1995
Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridizationE Blennow, K B Nielsen, H Telenius, et al.
American Journal of Human Genetics|May 1, 1994
Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNAE Blennow, H Telenius, D de Vos, et al.
Human Genetics|October 28, 1997
The germinal center kinase gene and a novel CDC25-like gene are located in the vicinity of the PYGM gene on 11q13D Kedra, E Seroussi, I Fransson, et al.
Genes, Chromosomes & Cancer|May 25, 1999
Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: possible localization of a neurofibromatosis type 2 modifier gene?C E Bruder, K Ichimura, E Blennow, et al.
Human Genetics|July 8, 1999
A high degree of aneuploidy in frozen-thawed human preimplantation embryosE Iwarsson, M Lundqvist, J Inzunza, et al.
Molecular Human Reproduction|October 23, 1998
Preimplantation genetic diagnosis of DiGeorge syndromeE Iwarsson, L Ahrlund-Richter, J Inzunza, et al.
Molecular Human Reproduction|August 14, 1998
Preimplantation genetic diagnosis of a large pericentric inversion of chromosome 5E Iwarsson, L Ahrlund-Richter, J Inzunza, et al.
American Journal of Human Genetics|February 27, 2001
Limitations of chromosome classification by multicolor karyotypingC Lee, D Gisselsson, C Jin, et al.
Clinical Genetics|October 30, 2009
Detailed molecular and clinical characterization of three patients with 21q deletionsA Lindstrand, H Malmgren, S Sahlén, et al.
Human Genetics|August 21, 2001
The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriersI Tapia-Páez, M Kost-Alimova, P Hu, et al.
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