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	1.	Genotype-Phenotype Relationship in Patients and Relatives with SHOX Region Anomalies in the French Population. [electronic resource] by Auger, Julie Baptiste, Amandine Benabbad, Imane Thierry, Gaëlle Costa, Jean-Marc Amouyal, Mélanie Kottler, Marie-Laure Leheup, Bruno Touraine, Renaud Schmitt, Sébastien Lebrun, Marine Cormier Daire, Valérie Bonnefont, Jean-Paul de Roux, Nicolas Elie, Caroline Rosilio, Myriam Producer: 20170417 In: Hormone research in paediatrics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	CoDE-seq, an augmented whole-exome sequencing, enables the accurate detection of CNVs and mutations in Mendelian obesity and intellectual disability. [electronic resource] by Montagne, Louise Derhourhi, Mehdi Piton, Amélie Toussaint, Bénédicte Durand, Emmanuelle Vaillant, Emmanuel Thuillier, Dorothée Gaget, Stefan De Graeve, Franck Rabearivelo, Iandry Lansiaux, Amélie Lenne, Bruno Sukno, Sylvie Desailloud, Rachel Cnop, Miriam Nicolescu, Ramona Cohen, Lior Zagury, Jean-François Amouyal, Mélanie Weill, Jacques Muller, Jean Sand, Olivier Delobel, Bruno Froguel, Philippe Bonnefond, Amélie Producer: 20190520 In: Molecular metabolism vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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