2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders.
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Genetics of Autism Spectrum Disorder: Current Status and Possible Clinical ApplicationsIdentifying candidate genes for 2p15p16.1 microdeletion syndrome using clinical, genomic, and functional analysis.Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders.Bio-collections in autism research.Genitourinary defects associated with genomic deletions in 2p15 encompassing OTX1.Biological significance of the importin-β family-dependent nucleocytoplasmic transport pathways.Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes.Neuropilin-2 rs849563 gene variations and susceptibility to autism in Iranian population: A case-control study.OTX1 regulates cell cycle progression of neural progenitors in the developing cerebral cortex.Complex craniosynostosis is associated with the 2p15p16.1 microdeletion syndrome
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2p15-p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
2p15-p16.1 microdeletion syndr ...... ith autism spectrum disorders.
@en
2p15-p16.1 microdeletion syndr ...... ith autism spectrum disorders.
@nl
type
label
2p15-p16.1 microdeletion syndr ...... ith autism spectrum disorders.
@en
2p15-p16.1 microdeletion syndr ...... ith autism spectrum disorders.
@nl
prefLabel
2p15-p16.1 microdeletion syndr ...... ith autism spectrum disorders.
@en
2p15-p16.1 microdeletion syndr ...... ith autism spectrum disorders.
@nl
P2093
P2860
P356
P1476
2p15-p16.1 microdeletion syndr ...... ith autism spectrum disorders.
@en
P2093
Albert E Chudley
Chansonette Harvard
Chelsea Reesor
Cynthia Forster-Gibson
Ira L Cohen
Jeanette J A Holden
M E Suzanne Lewis
Melissa L Hudson
Patrick Malenfant
P2860
P2888
P304
P356
10.1038/EJHG.2011.112
P577
2011-07-13T00:00:00Z