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	1.	Osteogenesis imperfecta, tricho-dento-osseous syndrome and intellectual disability: a familial case with 17q21.33-q22 (COL1A1 and DLX3) deletion and 7q32.3-q33 duplication resulting from a reciprocal interchromosomal insertion. [electronic resource] by Harbuz, Radu Bilan, Frédéric Couet, Dominique Charraud, Valérie Kitzis, Alain Gilbert-Dussardier, Brigitte Producer: 20140515 In: American journal of medical genetics. Part A vol. 161A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Association of structural and numerical anomalies of chromosome 22 in a patient with syndromic intellectual disability. [electronic resource] by Naoufal, Rania Legendre, Marine Couet, Dominique Gilbert-Dussardier, Brigitte Kitzis, Alain Bilan, Frederic Harbuz, Radu Producer: 20170202 In: European journal of medical genetics vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Complete screening of 50 patients with CHARGE syndrome for anomalies in the CHD7 gene using a denaturing high-performance liquid chromatography-based protocol: new guidelines and a proposal for routine diagnosis. [electronic resource] by Bilan, Frédéric Legendre, Marine Charraud, Valérie Manière, Barbara Couet, Dominique Gilbert-Dussardier, Brigitte Kitzis, Alain Producer: 20120403 In: The Journal of molecular diagnostics : JMD vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)