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

PGD for reciprocal and Robertsonian translocations using array comparative genomic hybridization

12 Apr 2011

Abstract excerpt

BACKGROUND: Fluorescence in situ hybridization (FISH) is the most widely used method for detecting unbalanced chromosome rearrangements in preimplantation embryos but it is known to have several technical limitations. We describe the clinical application of a molecular-based assay, array comparative genomic hybridization (array-CGH), to simultaneously screen for unbalanced translocation derivatives and aneuploidy...

Source

Identifiers

PMID: 21489979
DOI: 10.1093/humrep/der082

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

PGD for reciprocal and Robertsonian translocations using array comparative genomic hybridizationPMID 21489979Read ↗

First births after preimplantation genetic diagnosis of structural chromosome abnormalities using comparative genomic hybridization and microarray analysisSemantic proximity Read ↗

Preimplantation genetic diagnosis for chromosomal rearrangements with the use of array comparative genomic hybridization at the blastocyst stage.Semantic proximity Read ↗

Preimplantation Genetic Diagnosis for Aneuploidy and Translocations Using Array Comparative Genomic HybridizationSemantic proximity Read ↗

Use of comprehensive chromosomal screening for embryo assessment: microarrays and CGH.Semantic proximity Read ↗

Two different microarray technologies for preimplantation genetic diagnosis and screening, due to reciprocal translocation imbalances, demonstrate equivalent euploidy and clinical pregnancy rates.Semantic proximity Read ↗

Preliminary analysis of numerical chromosome abnormalities in reciprocal and Robertsonian translocation preimplantation genetic diagnosis cases with 24-chromosomal analysis with an aCGH/SNP microarray.Semantic proximity Read ↗

Validation of Next-Generation Sequencing and Array Comparative Genomic Hybridization for Diagnosis and Screening of Reciprocal and Robertsonian Translocations in Human BlastocystsSemantic proximity Read ↗

Cytogenetics in reproductive medicine: The contribution of comparative genomic hybridization (CGH)Semantic proximity Read ↗

Preimplantation Genetic Diagnosis—An OverviewSemantic proximity Read ↗

Validation of a semiconductor next‐generation sequencing‐based protocol for preimplantation genetic diagnosis of reciprocal translocationsSemantic proximity Read ↗

Application of next-generation sequencing technology for comprehensive aneuploidy screening of blastocysts in clinical preimplantation genetic screening cyclesSemantic proximity Read ↗

An overview of the current and emerging platforms for preimplantation genetic testing for aneuploidies (PGT-A) in in vitro fertilization programsSemantic proximity Read ↗

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