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	1.	Autosomal insertional translocation mimicking an X-linked mode of inheritance. [electronic resource] by Thierry, Gaelle Pichon, Olivier Briand, Annaig Poulain, Damien Sznajer, Yves David, Albert Le Caignec, Cédric Producer: 20130611 In: European journal of medical genetics vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Disruption of the SEMA3D gene in a patient with congenital heart defects. [electronic resource] by Sanchez-Castro, Marta Pichon, Olivier Briand, Annaig Poulain, Damien Gournay, Véronique David, Albert Le Caignec, Cédric Producer: 20150910 In: Human mutation vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mandibular dysostosis without microphthalmia caused by OTX2 deletion. [electronic resource] by Latypova, Xénia Bordereau, Sylvain Bleriot, Alice Pichon, Olivier Poulain, Damien Briand, Annaïg Le Caignec, Cédric Isidor, Bertrand Producer: 20171019 In: American journal of medical genetics. Part A vol. 170 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	De novo duplication and deletions at 7q in a three-generation family. [electronic resource] by Isidor, Bertrand Villa, Olaya Pichon, Olivier Briand, Annaig Poulain, Damien Boisseau, Pierre Pérez-Jurado, Luis Alberto Le Caignec, Cédric Producer: 20120924 In: American journal of medical genetics. Part A vol. 158A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Wilms' tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomas. [electronic resource] by Isidor, Bertrand Bourdeaut, Franck Lafon, Delfine Plessis, Ghislaine Lacaze, Elodie Kannengiesser, Caroline Rossignol, Sylvie Pichon, Olivier Briand, Annaig Martin-Coignard, Dominique Piccione, Maria David, Albert Delattre, Olivier Jeanpierre, Cécile Sévenet, Nicolas Le Caignec, Cédric Producer: 20131104 In: European journal of human genetics : EJHG vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Fryns type mesomelic dysplasia of the upper limbs caused by inverted duplications of the HOXD gene cluster. [electronic resource] by Le Caignec, Cédric Pichon, Olivier Briand, Annaig de Courtivron, Benoît Bonnard, Christian Lindenbaum, Pierre Redon, Richard Schluth-Bolard, Caroline Diguet, Flavie Rollat-Farnier, Pierre-Antoine Sanchez-Castro, Marta Vuillaume, Marie-Laure Sanlaville, Damien Duboule, Denis Mégarbané, André Toutain, Annick Producer: 20210430 In: European journal of human genetics : EJHG vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)