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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 VekemansOrphanet Journal of Rare Diseases|February 24, 2009
Distal Xq duplication and functional Xq disomyDamien Sanlaville, Caroline Schluth-Bolard, Catherine TurleauAmerican Journal of Medical Genetics. Part A|September 15, 2005
Intrachromosomal insertion mimicking a pericentric inversion: molecular cytogenetic characterization of a three break rearrangement of chromosome 20Azarnouche Ardalan, Marguerite Prieur, Agnès Choiset, et al.Cytogenetic 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.American Journal of Medical Genetics. Part A|December 14, 2011
An 800 kb deletion at 17q23.2 including the MED13 (THRAP1) gene, revealed by aCGH in a patient with a SMC 17pNadia Boutry-Kryza, Audrey Labalme, Marianne Till, et al.European Journal of Medical Genetics|September 24, 2005
Molecular karyotyping in human constitutional cytogeneticsDamien Sanlaville, Jean-Michel Lapierre, Catherine Turleau, et al.American Journal of Medical Genetics. Part A|April 14, 2007
De novo trisomy 20p of paternal originMyriam Chaabouni, Catherine Turleau, Lotfi Karboul, et al.Human Genetics|December 31, 2016
Aniridia, male pseudohermaphroditism, gonadoblastoma, mental retardation, and del 11p13Catherine Turleau, J de Grouchy, J L Dufier, et al.Pageof 3