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Cancer Genetics and Cytogenetics|July 30, 2003
Three new cases of non-Hodgkin lymphoma with t(9;14)(p13;q32)Joris Andrieux, Sandra Fert-Ferrer, Marie-Christine Copin, et al.
Endocrine Journal|July 2, 2011
Identification by array-Comparative Genomic Hybridization (array-CGH) of a large deletion of luteinizing hormone receptor gene combined with a missense mutation in a patient diagnosed with a 46,XY disorder of sex development and application to prenatal diagnosisNicolas Richard, Céline Leprince, Nicolas Gruchy, et al.
European Journal of Medical Genetics|December 15, 2010
A 5.3Mb deletion in chromosome 18q12.3 as the smallest region of overlap in two patients with expressive speech delaySonia Bouquillon, Joris Andrieux, Emilie Landais, et al.
European Journal of Medical Genetics|December 4, 2012
Split-hand/foot malformation with long-bone deficiency and BHLHA9 duplication: two cases and expansion of the phenotype to radial agenesisFlorence Petit, Joris Andrieux, Bénédicte Demeer, et al.
Genes, Chromosomes & Cancer|June 9, 2005
Familial occurrence of thymoma and autoimmune diseases with the constitutional translocation t(14;20)(q24.1;p12.3)Frédéric Nicodème, Sandrine Geffroy, Massimo Conti, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Interstitial 12p13.1 deletion involving GRIN2B in three patients with intellectual disabilitySarra Dimassi, Joris Andrieux, Audrey Labalme, et al.
European Journal of Human Genetics : EJHG|March 19, 2015
The disruption of a novel limb cis-regulatory element of SHH is associated with autosomal dominant preaxial polydactyly-hypertrichosisFlorence Petit, Anne-Sophie Jourdain, Muriel Holder-Espinasse, et al.
Annales De Genetique|October 17, 2002
TPA stimulation culture for improved detection of t(11;14)(q13;q32) in mantle cell lymphomaEmmanuelle Barouk-Simonet, Joris Andrieux, Marie-Christine Copin, et al.
Molecular Cytogenetics|November 14, 2009
A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case reportFrenny Sheth, Elisabeth Ewers, Nadezda Kosyakova, et al.
American Journal of Medical Genetics. Part A|November 28, 2014
Involvement of interstitial telomeric sequences in two new cases of mosaicism for autosomal structural rearrangementsJonathan Lévy, Aline Receveur, Guillaume Jedraszak, et al.
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