Copy number variants (CNVs) analysis in a deeply phenotyped cohort of individuals with intellectual disability (ID).
about
Clinically relevant copy number variations detected in cerebral palsyXp11.2 microduplications including IQSEC2, TSPYL2 and KDM5C genes in patients with neurodevelopmental disorders.Interactive Exploration, Analysis, and Visualization of Complex Phenome-Genome Datasets with ASPIREdbMolecular Characterization of Koolen De Vries Syndrome in Two Girls with Idiopathic Intellectual Disability from Central Brazil.
P2860
Copy number variants (CNVs) analysis in a deeply phenotyped cohort of individuals with intellectual disability (ID).
description
2014 nî lūn-bûn
@nan
2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Copy number variants (CNVs) an ...... intellectual disability (ID).
@ast
Copy number variants (CNVs) an ...... intellectual disability (ID).
@en
type
label
Copy number variants (CNVs) an ...... intellectual disability (ID).
@ast
Copy number variants (CNVs) an ...... intellectual disability (ID).
@en
prefLabel
Copy number variants (CNVs) an ...... intellectual disability (ID).
@ast
Copy number variants (CNVs) an ...... intellectual disability (ID).
@en
P2093
P2860
P356
P1433
P1476
Copy number variants (CNVs) an ...... intellectual disability (ID).
@en
P2093
Albert E Chudley
Barbara McGillivray
Eloi Mercier
Francois P Bernier
Jane Hurlburt
Jila Dastan
Me Suzanne Lewis
Sandra Farrell
P2860
P2888
P356
10.1186/1471-2350-15-82
P577
2014-07-16T00:00:00Z