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American Journal of Medical Genetics|February 13, 2002
Subtelomeric rearrangements detected in patients with idiopathic mental retardationBritt-Marie Anderlid, Jacqueline Schoumans, Göran Annerén, et al.
European Journal of Medical Genetics|January 5, 2010
22q11.2 microduplication in two patients with bladder exstrophy and hearing impairmentJohanna Lundin, Cilla Söderhäll, Lina Lundén, et al.
British Journal of Haematology|February 16, 2008
Array-CGH reveals hidden gene dose changes in children with acute lymphoblastic leukaemia and a normal or failed karyotype by G-bandingEkaterina Kuchinskaya, Mats Heyman, Ann Nordgren, et al.
Genes, Chromosomes & Cancer|January 17, 2016
Guidelines for genomic array analysis in acquired haematological neoplastic disordersJacqueline Schoumans, Javier Suela, Ros Hastings, et al.
European Journal of Human Genetics : EJHG|October 21, 2004
Genome-wide screening using array-CGH does not reveal microdeletions/microduplications in children with Kabuki syndromeJacqueline Schoumans, Ann Nordgren, Claudia Ruivenkamp, et al.
American Journal of Medical Genetics. Part A|April 4, 2003
Ten years follow up of a boy with a complex chromosomal rearrangement: going from a > 5 to 15-breakpoint CCRGunnar Houge, Thomas Liehr, Jacqueline Schoumans, et al.
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.
American Journal of Medical Genetics. Part A|November 19, 2009
Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsyYasemin Soysal, Sevim Balci, Kuyaş Hekimler, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
Detection of submicroscopic constitutional chromosome aberrations in clinical diagnostics: a validation of the practical performance of different array platformsZhong-Fa Zhang, Claudia Ruivenkamp, Johan Staaf, et al.
Scientific Reports|January 23, 2025
A de novo, mosaic and complex chromosome 21 rearrangement causes APP triplication and familial autosomal dominant early onset Alzheimer diseaseEmma Ehn, Jesper Eisfeldt, Jose M Laffita-Mesa, et al.
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