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Missense Variants in the Histone Acetyltransferase Complex ..:
Cogné, Benjamin
;
Ehresmann, Sophie
;
Beauregard-Lacroix, Eliane
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2019.01.010. , 2019
Link:
https://univ-rennes.hal.science/hal-02181523
RT Journal T1
Missense Variants in the Histone Acetyltransferase Complex Component Gene TRRAP Cause Autism and Syndromic Intellectual Disability
UL https://suche.suub.uni-bremen.de/peid=base-ftunivrennes1hal:oai:HAL:hal-02181523v1&Exemplar=1&LAN=DE A1 Cogné, Benjamin A1 Ehresmann, Sophie A1 Beauregard-Lacroix, Eliane A1 Rousseau, Justine A1 Besnard, Thomas A1 Garcia, Thomas A1 Petrovski, Slavé A1 Avni, Shiri A1 Mcwalter, Kirsty A1 Blackburn, Patrick A1 Sanders, Stephan A1 Uguen, Kévin A1 Harris, Jacqueline A1 Cohen, Julie A1 Blyth, Moira A1 Lehman, Anna A1 Berg, Jonathan A1 Li, Mindy A1 Kini, Usha A1 Joss, Shelagh A1 Lippe, Charlotte von Der A1 Gordon, Christopher A1 Humberson, Jennifer A1 Robak, Laurie, A A1 Scott, Daryl A1 Sutton, Vernon, R A1 Skraban, Cara A1 Johnston, Jennifer A1 Poduri, Anna A1 Nordenskjöld, Magnus A1 Shashi, Vandana A1 Gerkes, Erica A1 Bongers, Ernie M.H.F A1 Gilissen, Christian A1 Zarate, Yuri A1 Kvarnung, Malin A1 Lally, Kevin A1 Kulch, Peggy A1 Daniels, Brina A1 García, Andres A1 Stong, Nicholas A1 Mcgaughran, Julie A1 Retterer, Kyle A1 Tveten, Kristian A1 Sullivan, Jennifer A1 Geisheker, Madeleine A1 Stray-Pedersen, Asbjorg A1 Tarpinian, Jennifer A1 Klee, Eric A1 Sapp, Julie A1 Zyskind, Jacob A1 Holla, Øystein A1 Bedoukian, Emma A1 Filippini, Francesca A1 Guimier, Anne A1 Picard, Arnaud A1 Busk, Øyvind, Løvold A1 Punetha, Jaya A1 Pfundt, Rolph A1 Lindstrand, Anna, A A1 Nordgren, Ann, A A1 Kalb, Fayth A1 Desai, Megha A1 Ebanks, Ashley Harmon A1 Jhangiani, Shalini A1 Dewan, Tammie A1 Coban Akdemir, Zeynep A1 Telegrafi, Aida A1 Zackai, Elaine A1 Begtrup, Amber A1 Song, Xiaofei A1 Toutain, Ann A1 Wentzensen, Ingrid A1 Odent, Sylvie A1 Bonneau, Dominique A1 Latypova, Xenia A1 Deb, Wallid A1 Redon, Sylvia A1 Bilan, Frédéric A1 Legendre, Marine A1 Troyer, Caitlin A1 Whitlock, Kerri A1 Caluseriu, Oana A1 Murphree, Marine A1 Pichurin, Pavel A1 Agre, Katherine A1 Gavrilova, Ralitza A1 Rinne, Tuula A1 Park, Meredith A1 Shain, Catherine A1 Heinzen, Erin A1 Xiao, Rui A1 Amiel, Jeanne A1 Lyonnet, Stanislas A1 Isidor, Bertrand A1 Biesecker, Leslie A1 Lowenstein, Dan A1 Posey, Jennifer A1 Denommé-Pichon, Anne-Sophie A1 Férec, Claude A1 Yang, Xiang-Jiao A1 Rosenfeld, Jill, A A1 Gilbert-Dussardier, Brigitte A1 Audebert-Bellanger, Séverine A1 Redon, Richard A1 Stessman, Holly A.F A1 Nellaker, Christoffer A1 Yang, Yaping A1 Lupski, James, R A1 Goldstein, David A1 Eichler, Evan, E A1 Bolduc, Francois A1 Bézieau, Stéphane A1 Küry, Sébastien A1 Campeau, Philippe PB HAL CCSD; Elsevier (Cell Press) YR 2019 K1 neurodevelopmental disorders K1 intellectual disability K1 TRRAP K1 autism spectrum disorder K1 congenital malformations K1 de novo variants K1 histone acetylation K1 [SDV.GEN]Life Sciences [q-bio]/Genetics JF info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2019.01.010 LK http://dx.doi.org/https://univ-rennes.hal.science/hal-02181523 DO https://univ-rennes.hal.science/hal-02181523 SF ELIB - SuUB Bremen
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