Cogne, B., Beauregard-Lacroix, E., Rousseau, J., Ehresmann, S., Garcia, T., Gordon, C., … Campeau, P. M. (2019). Genotype-phenotype correlation associated with de novo missense variants in TRRAP: from autism spectrum disorder to syndromic intellectual disability. In EUROPEAN JOURNAL OF HUMAN GENETICS (Vol. 27, pp. 245–246). Milan, ITALY: NATURE PUBLISHING GROUP.

Cogne, B., E. Beauregard-Lacroix, J. Rousseau, S. Ehresmann, T. Garcia, C. Gordon, C. von der Lippe, et al. “Genotype-phenotype correlation associated with de novo missense variants in TRRAP: from autism spectrum disorder to syndromic intellectual disability.” In EUROPEAN JOURNAL OF HUMAN GENETICS, 27:245–46. NATURE PUBLISHING GROUP, 2019.

Cogne B, Beauregard-Lacroix E, Rousseau J, Ehresmann S, Garcia T, Gordon C, et al. Genotype-phenotype correlation associated with de novo missense variants in TRRAP: from autism spectrum disorder to syndromic intellectual disability. In: EUROPEAN JOURNAL OF HUMAN GENETICS. NATURE PUBLISHING GROUP; 2019. p. 245–6.

Cogne, B., et al. “Genotype-phenotype correlation associated with de novo missense variants in TRRAP: from autism spectrum disorder to syndromic intellectual disability.” EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 27, NATURE PUBLISHING GROUP, 2019, pp. 245–46.

Cogne B, Beauregard-Lacroix E, Rousseau J, Ehresmann S, Garcia T, Gordon C, von der Lippe C, Skraban C, Johnston J, Lehman A, Parent P, Gilbert-Dussardier B, McWalter K, Cho MT, Kini U, Akdemir ZC, Punetha J, Jhangiani S, Song X, Scott DA, Stray-Pedersen A, Blackburn P, Cohen JS, Stessman H, Blyth M, Berg J, Gerkes E, Shashi V, Sullivan J, Goldstein DB, Redon R, Lupski JR, Bolduc F, Bezieau S, Kury S, Campeau PM. Genotype-phenotype correlation associated with de novo missense variants in TRRAP: from autism spectrum disorder to syndromic intellectual disability. EUROPEAN JOURNAL OF HUMAN GENETICS. NATURE PUBLISHING GROUP; 2019. p. 245–246.