Genotype-phenotype correlation associated with de novo missense variants in TRRAP: from autism spectrum disorder to syndromic intellectual disability
Publication
, Conference
Cogne, B; Beauregard-Lacroix, E; Rousseau, J; Ehresmann, S; Garcia, T; Gordon, C; von der Lippe, C; Skraban, C; Johnston, J; Lehman, A; Cho, MT ...
Published in: EUROPEAN JOURNAL OF HUMAN GENETICS
July 1, 2019
Duke Scholars
Published In
EUROPEAN JOURNAL OF HUMAN GENETICS
EISSN
1476-5438
ISSN
1018-4813
Publication Date
July 1, 2019
Volume
27
Start / End Page
245 / 246
Location
Milan, ITALY
Publisher
NATURE PUBLISHING GROUP
Conference Name
51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG)
Related Subject Headings
- Genetics & Heredity
- 3202 Clinical sciences
- 3105 Genetics
- 1103 Clinical Sciences
- 0604 Genetics
Citation
APA
Chicago
ICMJE
MLA
NLM
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.
Published In
EUROPEAN JOURNAL OF HUMAN GENETICS
EISSN
1476-5438
ISSN
1018-4813
Publication Date
July 1, 2019
Volume
27
Start / End Page
245 / 246
Location
Milan, ITALY
Publisher
NATURE PUBLISHING GROUP
Conference Name
51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG)
Related Subject Headings
- Genetics & Heredity
- 3202 Clinical sciences
- 3105 Genetics
- 1103 Clinical Sciences
- 0604 Genetics