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

The use of arrays in preimplantation genetic diagnosis and screening.

Fertility and sterility - 1 Sept 2010

Harper Joyce C, Harton Gary

Abstract excerpt

BACKGROUND: In preimplantation genetic diagnosis (PGD), polymerase chain reaction has been used to detect monogenic disorders, and in PGD/preimplantation genetic screening (PGS), fluorescence in situ hybridization (FISH) has been used to analyze chromosomes. Ten randomized controlled trials (RCTs) using FISH-based PGS on cleavage-stage embryos and one on blastocyst-stage embryos have shown that PGS does not...

Read the complete abstract on PubMed

Topics

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

Share to Polymorphism, Single Nucleotide
Share to Comparative Genomic Hybridization
Share to PGD gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Models, Biological

Share to Oligonucleotide Array Sequence Analysis

Share to Pregnancy

Share to Preimplantation Diagnosis

Source

Identifiers

PMID: 20579641
DOI: 10.1016/j.fertnstert.2010.04.064

Genes

PGD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The use of arrays in preimplantation genetic diagnosis and screening.PMID 20579641Read ↗

Preimplantation genetic diagnosis: state of the art 2011.Semantic proximity Read ↗

What next for preimplantation genetic screening (PGS)? A position statement from the ESHRE PGD Consortium steering committeeSemantic proximity Read ↗

Preimplantation genetic screening: does it help or hinder IVF treatment and what is the role of the embryo?Semantic proximity Read ↗

An update of preimplantation genetic diagnosis in gene diseases, chromosomal translocation, and aneuploidy screeningSemantic proximity Read ↗

Preimplantation Genetic Diagnosis—An OverviewSemantic proximity Read ↗

What next for preimplantation genetic screening? High mitotic chromosome instability rate provides the biological basis for the low success rateSemantic proximity Read ↗

Preimplantation Genetic Diagnosis: Prenatal Testing for Embryos Finally Achieving Its PotentialSemantic proximity Read ↗

The role of preimplantation genetic diagnosis in diagnosing embryo aneuploidySemantic proximity Read ↗

Use of single nucleotide polymorphism microarrays to distinguish between balanced and normal chromosomes in embryos from a translocation carrier.Semantic proximity Read ↗

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

PGD for reciprocal and Robertsonian translocations using array comparative genomic hybridizationSemantic 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 ↗

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