Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of Cornelia de Lange syndrome with predominant mental retardation

DEARDORFF, MA; KAUR, M; YAEGER, D; RAMPURIA, A; KOROLEV, S; PIE, J; GIL-RODRIGUEZ, C; ARNEDO, M; Loeys, Bart; KLINE, AD; WILSON, M; LILLQUIST, K; SIU, V; RAMOS, FJ; MUSIO, A; JACKSON, LS; DORSETT, D; KRANTZ, ID

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oai:archive.ugent.be:390098

Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of Cornelia de Lange syndrome with predominant mental retardation

Authors: MA DEARDORFF
M KAUR
D YAEGER
A RAMPURIA
S KOROLEV
J PIE
C GIL-RODRIGUEZ
M ARNEDO
Bart Loeys
AD KLINE
M WILSON
K LILLQUIST
V SIU
FJ RAMOS
A MUSIO
LS JACKSON
D DORSETT
ID KRANTZ
Publication date: 1 January 2007
Publisher: UNIV CHICAGO PRESS
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oai:archive.ugent.be:390098

Last time updated on 12/11/2016

This paper was published in Ghent University Academic Bibliography.

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