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Evica Rajcan-Separovic

University of British Columbia
H指数:33
被引数:3,787

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A genome-wide DNA methylation signature for SETD1B-related syndrome
2019-11-0446
OAAI
Identifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysis
2016-03-1732
OA
Variant ATRX Syndrome with Dysfunction of ATRX and MAGT1 Genes
2013-11-1010
PREAI
Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2

由于2 p13.2的反复微缺失,胞吐和视黄酸途径的基因单倍体不足的表型和功能后果

2013-07-1024
OAAI
Understanding the impact of 1q21.1 copy number variant
2011-08-0850
OAAI
Genomic and clinical characteristics of six patients with partially overlapping interstitial deletions at 10p12p11
2011-04-2725
OAAI
Disruption at the PTCHD1 Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability
2010-09-15188
OAAI