(Q36662408)

15 August 2017

1 reference

title

Idiopathic learning disability and genome imbalance (English)

1 reference

15 August 2017

0 references

1 reference

Knight SJ

1

1 reference

15 August 2017

Regan R

series ordinal

2

1 reference

15 August 2017

publication date

1 January 2006

1 reference

Cytogenetics and Genome Research

15 August 2017

published in

1 reference

15 August 2017

volume

115

1 reference

15 August 2017

issue

3-4

1 reference

15 August 2017

page(s)

215-224

1 reference

Subtelomeric rearrangements detected in patients with idiopathic mental retardation

15 August 2017

cites work

1 reference

Use of primed in situ labeling (PRINS) for the detection of telomeric deletions associated with mental retardation.

21 January 2018

1 reference

Diagnostic genome profiling in mental retardation

21 January 2018

1 reference

Recent duplication, domain accretion and the dynamic mutation of the human genome

21 January 2018

1 reference

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

21 January 2018

1 reference

Detection of large-scale variation in the human genome

21 January 2018

1 reference

Perfect endings: a review of subtelomeric probes and their use in clinical diagnosis

21 January 2018

1 reference

A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism.

21 January 2018

1 reference

Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities

21 January 2018

1 reference

Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents

21 January 2018

1 reference

Large-scale copy number polymorphism in the human genome

21 January 2018

1 reference

Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

21 January 2018

1 reference

Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

21 January 2018

1 reference

Molecular-evolutionary mechanisms for genomic disorders

21 January 2018

1 reference

A common inversion under selection in Europeans

21 January 2018

1 reference

Fine-scale structural variation of the human genome

21 January 2018

1 reference

Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1159/000095917

1 reference

15 August 2017

1 reference