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	1.	Identification of rare copy number variations reveals PJA2, APCS, SYNPO, and TAC1 as novel candidate genes in Autism Spectrum Disorders. [electronic resource] by Bitar, Tania Hleihel, Walid Marouillat, Sylviane Vonwill, Sandrine Vuillaume, Marie-Laure Soufia, Michel Vourc'h, Patrick Laumonnier, Frederic Andres, Christian R Producer: 20200626 In: Molecular genetics & genomic medicine vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Mutation update for the GPC3 gene involved in Simpson-Golabi-Behmel syndrome and review of the literature. [electronic resource] by Vuillaume, Marie-Laure Moizard, Marie-Pierre Rossignol, Sylvie Cottereau, Edouard Vonwill, Sandrine Alessandri, Jean-Luc Busa, Tiffany Colin, Estelle Gérard, Marion Giuliano, Fabienne Lambert, Laetitia Lefevre, Mathilde Kotecha, Udhaya Nampoothiri, Sheela Netchine, Irène Raynaud, Martine Brioude, Frédéric Toutain, Annick Publication details: Human mutation Dec 2018 In: Human mutation vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mutation update for the GPC3 gene involved in Simpson-Golabi-Behmel syndrome and review of the literature. [electronic resource] by Vuillaume, Marie-Laure Moizard, Marie-Pierre Rossignol, Sylvie Cottereau, Edouard Vonwill, Sandrine Alessandri, Jean-Luc Busa, Tiffany Colin, Estelle Gérard, Marion Giuliano, Fabienne Lambert, Laetitia Lefevre, Mathilde Kotecha, Udhaya Nampoothiri, Sheela Netchine, Irène Raynaud, Martine Brioude, Frédéric Toutain, Annick Producer: 20190530 In: Human mutation vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)