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Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.
50 auth.
A. Bassett,
Chelsea Lowther,
D. Merico,
Gregory Costain,
E. Chow,
Thérèse Van Amelsvoort,
D. McDonald-McGinn,
R. Gur,
A. Swillen,
M. V. D. van den Bree,
K. Murphy,
D. Gothelf,
C. Bearden,
S. Eliez,
W. Kates,
...
N. Philip,
V. Sashi,
L. Campbell,
J. Vorstman,
J. Cubells,
G. Repetto,
T. Simon,
E. Boot,
T. Heung,
Rens Evers,
C. Vingerhoets,
E. V. van Duin,
E. Zackai,
E. Vergaelen,
K. Devriendt,
J. Vermeesch,
M. Owen,
C. Murphy,
Elena Michaelovosky,
L. Kushan,
Maude Schneider,
W. Fremont,
T. Busa,
S. Hooper,
K. McCabe,
Sasja N. Duijff,
K. Isaev,
G. Pellecchia,
John Wei,
Matthew J. Gazzellone,
S. Scherer,
B. Emanuel,
T. Guo,
B. Morrow,
C. Marshall
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6 |
2017 |
6
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