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1 Ergebnisse
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Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk ..:
Huang, Alden Y
;
Yu, Dongmei
;
Davis, Lea K
...
0896-6273. , 2017
Link:
https://dspace.library.uu.nl/handle/1874/361252
RT Journal T1
Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome
UL https://suche.suub.uni-bremen.de/peid=base-ftunivutrecht:oai:dspace.library.uu.nl:1874_361252&Exemplar=1&LAN=DE A1 Huang, Alden Y A1 Yu, Dongmei A1 Davis, Lea K A1 Sul, Jae Hoon A1 Tsetsos, Fotis A1 Ramensky, Vasily A1 Zelaya, Ivette A1 Ramos, Eliana Marisa A1 Osiecki, Lisa A1 Chen, Jason A A1 McGrath, Lauren M A1 Illmann, Cornelia A1 Sandor, Paul A1 Barr, Cathy L A1 Grados, Marco A A1 Singer, Harvey S A1 Nöthen, Markus M A1 Hebebrand, Johannes A1 King, Robert A A1 Dion, Yves A1 Rouleau, Guy A A1 Budman, Cathy L A1 Depienne, Christel A1 Worbe, Yulia A1 Hartmann, Andreas A1 Müller-Vahl, Kirsten R A1 Stuhrmann, Manfred A1 Aschauer, Harald A1 Stamenkovic, Mara A1 Schloegelhofer, Monika A1 Konstantinidis, Anastasios A1 Lyon, Gholson J A1 McMahon, William M A1 Barta, Csaba A1 Tarnok, Zsanett A1 Nagy, Peter A1 Batterson, James R A1 Rizzo, Renata A1 Cath, Danielle C A1 Wolanczyk, Tomasz A1 Berlin, Cheston A1 Malaty, Irene A A1 Okun, Michael S A1 Woods, Douglas W A1 Rees, Elliott A1 Pato, Carlos N A1 Pato, Michele T A1 Knowles, James A A1 Posthuma, Danielle A1 Smit, Jan A1 The Tourette Syndrome Association International Consortium for Genetics (TSAICG) A1 The Gilles de la Tourette Syndrome GWAS Replication Initiative (GGRI) YR 2017 K1 CNTN6 K1 copy number variation K1 genetics K1 neurodevelopmental disorders K1 NRXN1 K1 structural variation K1 tic disorders K1 Tourette Syndrome K1 Taverne K1 General Neuroscience JF 0896-6273 LK http://dx.doi.org/https://dspace.library.uu.nl/handle/1874/361252 DO https://dspace.library.uu.nl/handle/1874/361252 SF ELIB - SuUB Bremen
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