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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 17, 2013
Early telomere shortening and genomic instability in tubo-ovarian preneoplastic lesionsGautier Chene, Andrei Tchirkov, Eleonore Pierre-Eymard, et al.
European Journal of Medical Genetics|July 17, 2012
An atypical 0.8 Mb inherited duplication of 22q11.2 associated with psychomotor impairmentCéline Pebrel-Richard, Stéphan Kemeny, Laetitia Gouas, et al.
European Journal of Medical Genetics|August 10, 2014
Clinical and molecular description of a 17q21.33 microduplication in a girl with severe kyphoscoliosis and developmental delayStéphan Kemeny, Céline Pebrel-Richard, Eléonore Eymard-Pierre, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 11, 2010
Prenatal detection of cryptic rearrangements by multiplex ligation probe amplification in fetuses with ultrasound abnormalitiesCarole Goumy, Laetitia Gouas, Céline Pebrel-Richard, et al.
Prenatal Diagnosis|April 6, 2004
Chorionic villus sampling (CVS) and fluorescence in situ hybridization (FISH) for a rapid first-trimester prenatal diagnosisCarole Goumy, Marie-Noëlle Bonnet-Dupeyron, Yoan Cherasse, et al.
Chromosoma|December 15, 2017
Spatial organization of chromosome territories in the interphase nucleus of trisomy 21 cellsStephan Kemeny, Christophe Tatout, Gaelle Salaun, et al.
Annales De Biologie Clinique|September 16, 2020
Analysis of the cost effectiveness of different strategies for the antenatal diagnosis of chromosomal aberrations in cases of ultrasound-identified fetal abnormalitiesCharline Mourgues, Eléonore Eymard-Pierre, Hélène Laurichesse-Delmas, et al.
Reproductive Biomedicine Online|April 23, 2018
Sperm meiotic segregation of a balanced interchromosomal reciprocal insertion resulting in recurrent spontaneous miscarriageGaëlle Salaun, Andrei Tchirkov, Christine Francannet, et al.
Annales De Pathologie|July 19, 2002
[Interphase FISH analysis on histologic sections of fixed tissues for t(11;14) (q13;q32) detection in mantle cell lymphoma and t(8;14)(q24;q32) in Burkitt's lymphoma]Marc-Antoine Belaud-Rotureau, Marie Parrens, Pierre Dubus, et al.
European Journal of Medical Genetics|July 12, 2021
Further refining the critical region of 10q26 microdeletion syndrome: A possible involvement of INSYN2 and NPS in the cognitive phenotypeFlorian Cherik, Mathis Lepage, Ganaelle Remerand, et al.
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