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                                       Details for article 15 of 21 found articles
 
 
  Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome
 
 
Title: Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome
Author: Huang, Alden Y.
Yu, Dongmei
Davis, Lea K.
Sul, Jae Hoon
Tsetsos, Fotis
Ramensky, Vasily
Zelaya, Ivette
Ramos, Eliana Marisa
Osiecki, Lisa
Chen, Jason A.
McGrath, Lauren M.
Illmann, Cornelia
Sandor, Paul
Barr, Cathy L.
Grados, Marco
Singer, Harvey S.
Nöthen, Markus M.
Hebebrand, Johannes
King, Robert A.
Dion, Yves
Rouleau, Guy
Budman, Cathy L.
Depienne, Christel
Worbe, Yulia
Hartmann, Andreas
Müller-Vahl, Kirsten R.
Stuhrmann, Manfred
Aschauer, Harald
Stamenkovic, Mara
Schloegelhofer, Monika
Konstantinidis, Anastasios
Lyon, Gholson J.
McMahon, William M.
Barta, Csaba
Tarnok, Zsanett
Nagy, Peter
Batterson, James R.
Rizzo, Renata
Cath, Danielle C.
Wolanczyk, Tomasz
Berlin, Cheston
Malaty, Irene A.
Okun, Michael S.
Woods, Douglas W.
Rees, Elliott
Pato, Carlos N.
Pato, Michele T.
Knowles, James A.
Posthuma, Danielle
Pauls, David L.
Cox, Nancy J.
Neale, Benjamin M.
Freimer, Nelson B.
Paschou, Peristera
Mathews, Carol A.
Scharf, Jeremiah M.
Coppola, Giovanni
Appeared in: Neuron
Paging: Volume 94 (2017) nr. 6 pages 1101-1111.e7
Year: 2017
Contents:
Publisher: Elsevier Inc.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 15 of 21 found articles
 
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