(Q43170661)

English

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

scientific article published on 24 June 2005

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scholarly article

1 reference

Europe PubMed Central

15 November 2017

0 references

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

1 reference

Europe PubMed Central

15 November 2017

Jeroen Knijnenburg

2

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Europe PubMed Central

15 November 2017

14

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Europe PubMed Central

15 November 2017

object named as

E Bakker

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author name string

C Rosenberg

1

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Europe PubMed Central

15 November 2017

A M Vianna-Morgante

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Europe PubMed Central

15 November 2017

W Sloos

5

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Europe PubMed Central

15 November 2017

P A Otto

6

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Europe PubMed Central

15 November 2017

M Kriek

7

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Europe PubMed Central

15 November 2017

K Hansson

8

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Europe PubMed Central

15 November 2017

A C V Krepischi-Santos

9

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Europe PubMed Central

15 November 2017

H Fiegler

10

1 reference

Europe PubMed Central

15 November 2017

N P Carter

11

1 reference

Europe PubMed Central

15 November 2017

E K Bijlsma

12

1 reference

Europe PubMed Central

15 November 2017

A van Haeringen

13

1 reference

Europe PubMed Central

15 November 2017

H J Tanke

15

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Europe PubMed Central

15 November 2017

language of work or name

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publication date

24 June 2005

1 reference

Europe PubMed Central

15 November 2017

Journal of Medical Genetics

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Europe PubMed Central

15 November 2017

43

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2

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15 November 2017

180-186

1 reference

Europe PubMed Central

15 November 2017

Microduplication and triplication of 22q11.2: a highly variable syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564641

25 May 2018

Detection of large-scale variation in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564641

25 May 2018

Large-scale copy number polymorphism in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564641

25 May 2018

Genomic imbalances in mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564641

25 May 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564641

25 May 2018

Replication timing of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564641

25 May 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564641

25 May 2018

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564641

25 May 2018

DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564641

25 May 2018

Measurement of locus copy number by hybridisation with amplifiable probes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564641

25 May 2018

Subtle chromosomal rearrangements in children with unexplained mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564641

25 May 2018

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564641

25 May 2018

Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564641

25 May 2018

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564641

25 May 2018

Subtelomeric 6p deletion: clinical, FISH, and array CGH characterization of two cases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564641

15 August 2018

FOXC1 gene deletion is associated with eye anomalies in ring chromosome 6.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564641

15 August 2018

The use of telomere probes to investigate submicroscopic rearrangements associated with mental retardation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564641

15 August 2018

Comparative analysis of comparative genomic hybridization microarray technologies: report of a workshop sponsored by the Wellcome Trust.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2564641

15 August 2018

Genomic segmental polymorphisms in inbred mouse strains

1 reference

https://pubmed.ncbi.nlm.nih.gov/15980116

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Insights from genomic microarrays into structural chromosome rearrangements

1 reference

https://pubmed.ncbi.nlm.nih.gov/15980116

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.2005.032268

1 reference

Europe PubMed Central

15 November 2017

1 reference

Europe PubMed Central

15 November 2017

1 reference

Europe PubMed Central

15 November 2017

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