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Genome Medicine|July 31, 2010
Piecing together the problems in diagnosing low-level chromosomal mosaicismCaroline Robberecht, Jean-Pierre Fryns, Joris Robert VermeeschGenetics in Medicine : Official Journal of the American College of Medical Genetics|July 21, 2009
Diagnosis of miscarriages by molecular karyotyping: benefits and pitfallsCaroline Robberecht, Vicky Schuddinck, Jean-Pierre Fryns, et al.Prenatal Diagnosis|July 6, 2012
Cytogenetic and morphological analysis of early products of conception following hystero-embryoscopy from couples with recurrent pregnancy lossCaroline Robberecht, Anne Pexsters, Jan Deprest, et al.European Journal of Medical Genetics|March 11, 2009
Bronchiectasis and immune deficiency in an adult patient with deletion 2q37 due to an unbalanced translocation t(2;10)Irina Balikova, Joris Robert Vermeesch, Jean-Pierre Fryns, et al.Journal of Medical Genetics|July 9, 2010
Genomic rearrangements of the GREM1-FMN1 locus cause oligosyndactyly, radio-ulnar synostosis, hearing loss, renal defects syndrome and Cenani--Lenz-like non-syndromic oligosyndactylyBoyan Ivanov Dimitrov, Thierry Voet, Luc De Smet, et al.Human Mutation|January 12, 2005
Large deletions of the APC gene in 15% of mutation-negative patients with classical polyposis (FAP): a Belgian studyGeneviève Michils, Sabine Tejpar, Reinhilde Thoelen, et al.American Journal of Ophthalmology|March 1, 2011
High frequency of submicroscopic chromosomal deletions in patients with idiopathic congenital eye malformationsIrina Balikova, Thomy de Ravel, Carmen Ayuso, et al.Journal of Medical Genetics|December 19, 2006
Molecular characterisation of a mosaicism with a complex chromosome rearrangement: evidence for coincident chromosome healing by telomere capture and neo-telomere formationElyes Chabchoub, Laura Rodríguez, Enrique Galán, et al.Molecular Cytogenetics|April 12, 2012
Meiotic errors followed by two parallel postzygotic trisomy rescue events are a frequent cause of constitutional segmental mosaicismCaroline Robberecht, Thierry Voet, Gülen E Utine, et al.Human Molecular Genetics|May 13, 2005
Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosisHilde Van Esch, Karen Hollanders, Liesbeth Badisco, et al.Pageof 27