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	1.	Prenatal diagnosis of common aneuploidies using multiplex quantitative fluorescent polymerase chain reaction. [electronic resource] by El Mouatassim, S Becker, M Kuzio, S Ronsin, C Gil, S Nouchy, M Druard, L Forestier, F Producer: 20050210 In: Fetal diagnosis and therapy vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Skin pigmentary anomalies and mosaicism for an acentric marker chromosome originating from 3q. [electronic resource] by Portnoï, M F Boutchneï, S Bouscarat, F Morlier, G Nizard, S Dersarkissian, H Crickx, B Nouchy, M Taillemite, J L Belaich, S Producer: 19990611 In: Journal of medical genetics vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	3.	Molecular cytogenetic analysis of a duplication Xp in a female with an abnormal phenotype and random X inactivation. [electronic resource] by Portnoï, M F Bouayed-Abdelmoula, N Mirc, M Zemni, R Castaing, H Stephann, J Ardalan, A Vialard, F Nouchy, M Daoud, P Chelly, J Taillemite, J L Producer: 20010125 In: Clinical genetics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Cytogenetic and array-CGH characterization of a 6q27 deletion in a patient with developmental delay and features of Ehlers-Danlos syndrome. [electronic resource] by Mosca, A L Callier, P Masurel-Paulet, A Thauvin-Robinet, C Marle, N Nouchy, M Huet, F Dipanda, D De Paepe, A Coucke, P Mugneret, F Faivre, L Producer: 20100812 In: American journal of medical genetics. Part A vol. 152A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)