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European Journal of Medical Genetics|May 9, 2008
Characterization by array-CGH of an interstitial de novo tandem 6p21.2p22.1 duplication in a boy with epilepsy and developmental delayJoris Andrieux, Steven Richebourg, Bénédicte Duban-Bedu, et al.Cancer Genetics and Cytogenetics|December 21, 2005
Cryptic 6p21.3 duplications and triplication involving HMGA1 partially masked by add 6p in four cases of myelodysplasiaJoris Andrieux, Sandrine Geffroy, Chrystèle Bilhou-Nabera, et al.Cancer Genetics and Cytogenetics|October 16, 2002
Frequency of structural abnormalities of the long arm of chromosome 12 in myelofibrosis with myeloid metaplasiaJoris Andrieux, Jean Loup Demory, Pierre Morel, et al.Epilepsia Open|March 29, 2018
Partial deletion of DEPDC5 in a child with focal epilepsyMaria Clara Bonaglia, Roberto Giorda, Roberta Epifanio, et al.European Journal of Medical Genetics|July 5, 2011
7 Mb de novo deletion within 8q21 in a patient with distal arthrogryposis type 2B (DA2B)Kristin Hofmann, Jutta Becker, Raoul Heller, et al.Blood|May 22, 2012
On the role of FAN1 in Fanconi anemiaJuan P Trujillo, Leonardo B Mina, Roser Pujol, et al.European Journal of Medical Genetics|November 25, 2010
Crane-Heise syndrome: two further case reportsFlorence Petit, Louise Devisme, Annick Toutain, et al.European Journal of Medical Genetics|December 7, 2007
A 6.9 Mb 1qter deletion/4.4 Mb 18pter duplication in a boy with extreme microcephaly with simplified gyral pattern, vermis hypoplasia and corpus callosum agenesisJoris Andrieux, Jean-Christophe Cuvellier, Bénédicte Duban-Bedu, et al.American Journal of Medical Genetics. Part A|July 22, 2014
Whole ARX gene duplication is compatible with normal intellectual developmentCornel Popovici, Tiffany Busa, Odile Boute, et al.Genes, Chromosomes & Cancer|November 7, 2003
Dysregulation and overexpression of HMGA2 in myelofibrosis with myeloid metaplasiaJoris Andrieux, Jean-Loup Demory, Brigitte Dupriez, et al.Pageof 13