Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome (vol 74, pg 1286, 2004)

被引:36
作者
Fernandez, Thomas
Morgan, Thomas
Davis, Nicole
Klin, Ami
Morris, Ashley
Farhi, Anita
Lifton, Richard P.
State, Matthew W.
机构
关键词
D O I
10.1016/j.ajhg.2008.04.021
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
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页码:1385 / 1385
页数:1
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共 4 条
[1]   Molecular cytogenetic analysis and resequencing of Contactin Associated Protein-Like 2 in autism spectrum disorders [J].
Bakkaloglu, Betul ;
O'Roak, Brian J. ;
Louvi, Angeliki ;
Gupta, Abha R. ;
Abelson, Jesse E. ;
Morgan, Thomas M. ;
Chawarska, Katarzyna ;
Klin, Ami ;
Ercan-Sencicek, A. Gulhan ;
Stillman, Althea A. ;
Tanriover, Gamze ;
Abrahams, Brett S. ;
Duvall, Jackie A. ;
Robbins, Elissa M. ;
Geschwind, Daniel H. ;
Biederer, Thomas ;
Gunel, Murat ;
Lifton, Richard P. ;
State, Matthew W. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 82 (01) :165-173
[2]   Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome [J].
Fernandez, T ;
Morgan, T ;
Davis, N ;
Klin, A ;
Morris, A ;
Farhi, A ;
Lifton, RP ;
State, MW .
AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 74 (06) :1286-1293
[3]  
ROOHI J, 2008, J MED GENET IN PRESS
[4]   Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2 [J].
Strauss, KA ;
Puffenberger, EG ;
Huentelman, MJ ;
Gottlieb, S ;
Dobrin, SE ;
Parod, JM ;
Stephan, DA ;
Morton, DH .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (13) :1370-1377