about
Molecular cytogenetics and cytogenomics of brain diseases.High proportion of 22q13 deletions and SHANK3 mutations in Chinese patients with intellectual disabilityMolecular cytogenetic diagnosis and somatic genome variations.Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United Kingdom.Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation.Genetics and the general physician: insights, applications and future challenges.Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects.Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies.
P2860
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P2860
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Idiopathic learning disability and genome imbalance.
@ast
Idiopathic learning disability and genome imbalance.
@en
type
label
Idiopathic learning disability and genome imbalance.
@ast
Idiopathic learning disability and genome imbalance.
@en
prefLabel
Idiopathic learning disability and genome imbalance.
@ast
Idiopathic learning disability and genome imbalance.
@en
P2860
P356
P1476
Idiopathic learning disability and genome imbalance.
@en
P2093
P2860
P304
P356
10.1159/000095917
P577
2006-01-01T00:00:00Z