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Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qterThe recurrence risk of genetic complex diseases.Value for money? Array genomic hybridization for diagnostic testing for genetic causes of intellectual disability.In search of the MRX genes.Chromosome abnormality rate among Iranian patients with idiopathic mental retardation from consanguineous marriages.Mutations in ionotropic AMPA receptor 3 alter channel properties and are associated with moderate cognitive impairment in humans.X linked mental retardation: a clinical guide.A rational approach to the child with mental retardation for the paediatricianUnlocking Mendelian disease using exome sequencing.Positron emission tomography-computer tomography scan used as a monitoring tool following cellular therapy in cerebral palsy and mental retardation-a case report.Monogenic X-linked mental retardation: is it as frequent as currently estimated? The paradox of the ARX (Aristaless X) mutations.A rational approach to the child with mental retardation for the paediatrician
P2860
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P2860
description
1998 nî lūn-bûn
@nan
1998 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի մարտին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Recurrence risks in mental retardation
@ast
Recurrence risks in mental retardation
@en
type
label
Recurrence risks in mental retardation
@ast
Recurrence risks in mental retardation
@en
prefLabel
Recurrence risks in mental retardation
@ast
Recurrence risks in mental retardation
@en
P2860
P356
P1476
Recurrence risks in mental retardation
@en
P2093
J L Tolmie
P2860
P304
P356
10.1136/JMG.35.3.177
P407
P577
1998-03-01T00:00:00Z