(Q34584307)

3 August 2017

1 reference

title

Medical applications of array CGH and the transformation of clinical cytogenetics (English)

1 reference

3 August 2017

1 reference

Shaffer LG

1

1 reference

PubMed ID

17124414

3 August 2017

Bejjani BA

series ordinal

2

1 reference

PubMed ID

17124414

3 August 2017

language of work or name

1 reference

1 January 2006

1 reference

Cytogenetics and Genome Research

3 August 2017

1 reference

3 August 2017

115

1 reference

3 August 2017

303-309

1 reference

3 August 2017

3-4

1 reference

Diagnostic genome profiling in mental retardation

3 August 2017

1 reference

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

21 January 2018

1 reference

1-Mb resolution array-based comparative genomic hybridization using a BAC clone set optimized for cancer gene analysis

21 January 2018

1 reference

Detection of large-scale variation in the human genome

21 January 2018

1 reference

High resolution comparative genomic hybridisation in clinical cytogenetics

21 January 2018

1 reference

Subtle chromosomal rearrangements in children with unexplained mental retardation

21 January 2018

1 reference

Comparative genomic hybridization: uses and limitations

21 January 2018

1 reference

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

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

Assembly of microarrays for genome-wide measurement of DNA copy number

21 January 2018

1 reference

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

21 January 2018

1 reference

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1159/000095928

1 reference

3 August 2017

1 reference

PubMed ID

17124414