Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Molecular Karyotyping: Array CGH Quality Criteria for Constitutional Genetic Diagnosis

1 Mar 2005

Abstract excerpt

Array CGH (comparative genomic hybridization) enables the identification of chromosomal copy number changes. The availability of clone sets covering the human genome opens the possibility for the widespread use of array CGH for both research and diagnostic purposes. In this manuscript we report on the parameters that were critical for successful implementation of the technology, assess quality criteria, and...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chromosomal and Genetic Variations
Share to Genomic variations and chromosomal abnormalities
Share to Prenatal Screening and Diagnostics

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 15750031
DOI: 10.1369/jhc.4a6436.2005

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular Karyotyping: Array CGH Quality Criteria for Constitutional Genetic DiagnosisPMID 15750031Read ↗

Clinical utility of contemporary molecular cytogenetics.Semantic proximity Read ↗

Cytogenetics in the genomics era: why karyotyping still mattersSemantic proximity Read ↗

Guidelines for molecular karyotyping in constitutional genetic diagnosisSemantic proximity Read ↗

American College of Medical Genetics recommendations for the design and performance expectations for clinical genomic copy number microarrays intended for use in the postnatal setting for detection of constitutional abnormalitiesSemantic proximity Read ↗

ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013.Semantic proximity Read ↗

Human molecular cytogenetics: from cells to nucleotidesSemantic proximity Read ↗

[Diagnosis of chromosomal abnormalities by array CGH in constitutional pathology: the end of the first-line karyotype].Semantic proximity Read ↗

Development and validation of a CGH microarray for clinical cytogenetic diagnosisSemantic proximity Read ↗

Detection of Chromosomal Aberrations in Clinical Practice: From Karyotype to Genome SequenceSemantic proximity Read ↗

Copy number variations and clinical cytogenetic diagnosis of constitutional disorders.Semantic proximity Read ↗

[Revolutionary progress and clinical application of digital karyotyping by array-CGH].Semantic proximity Read ↗

Molecular karyotyping: from microscope to SNP arrays.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.