Towards identification of individual etiologies by resolving genomic and biological conundrums in patients with autism spectrum disorders.
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Mechanisms of Origin, Phenotypic Effects and Diagnostic Implications of Complex Chromosome RearrangementsConnecting the CNTNAP2 Networks with Neurodevelopmental DisordersA candidate gene association study further corroborates involvement of contactin genes in autismMicrodeletions including FMR1 in three female patients with intellectual disability - further delineation of the phenotype and expression studies.Late breaking chromosomes.The Relationship of HLA Class I and II Alleles and Haplotypes with Autism: A Case Control Study.Late breaking chromosomes.SHANK Mutations May Disorder Brain Development.The Age of the Father.
P2860
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P2860
Towards identification of individual etiologies by resolving genomic and biological conundrums in patients with autism spectrum disorders.
description
2013 nî lūn-bûn
@nan
2013 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Towards identification of indi ...... ith autism spectrum disorders.
@ast
Towards identification of indi ...... ith autism spectrum disorders.
@en
type
label
Towards identification of indi ...... ith autism spectrum disorders.
@ast
Towards identification of indi ...... ith autism spectrum disorders.
@en
prefLabel
Towards identification of indi ...... ith autism spectrum disorders.
@ast
Towards identification of indi ...... ith autism spectrum disorders.
@en
P2860
P356
P1476
Towards identification of indi ...... ith autism spectrum disorders.
@en
P2093
P2860
P304
P356
10.1159/000350041
P577
2013-04-04T00:00:00Z