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Medecine Sciences : M/S|November 9, 2005
[New developments in cytogenetics]Catherine Turleau, Michel VekemansMedecine Sciences : M/S|March 30, 2010
[Trisomy 21: fifty years between medicine and science]Catherine Turleau, Michel VekemansCytogenetic and Genome Research|March 9, 2017
Large Duplications Can Be Benign Copy Number Variants: A Case of a 3.6-Mb Xq21.33 DuplicationMarie-Laure Maurin, Chloé Arfeuille, Pascale Sonigo, et al.European Journal of Medical Genetics|September 24, 2005
Molecular karyotyping in human constitutional cytogeneticsDamien Sanlaville, Jean-Michel Lapierre, Catherine Turleau, et al.European Journal of Human Genetics : EJHG|October 22, 2009
Familial interstitial Xq27.3q28 duplication encompassing the FMR1 gene but not the MECP2 gene causes a new syndromic mental retardation conditionMarlène Rio, Valérie Malan, Sarah Boissel, et al.Orphanet Journal of Rare Diseases|February 24, 2009
Distal Xq duplication and functional Xq disomyDamien Sanlaville, Caroline Schluth-Bolard, Catherine TurleauCytogenetic and Genome Research|November 18, 2014
17q21.31 microdeletion: brain anomalies leading to prenatal diagnosisMatthieu Egloff, Ferechte Encha-Razavi, Catherine Garel, et al.European Journal of Human Genetics : EJHG|October 22, 2009
Array-based comparative genomic hybridization identifies a high frequency of copy number variations in patients with syndromic overgrowthValérie Malan, Suzanne Chevallier, Gwendoline Soler, et al.European Journal of Human Genetics : EJHG|October 31, 2002
Overgrowth and trisomy 15q26.1-qter including the IGF1 receptor gene: report of two families and review of the literatureLaurence Faivre, Philippe Gosset, Valérie Cormier-Daire, et al.Pageof 11