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

Familial haplotyping and embryo analysis for Preimplantation genetic diagnosis (PGD) using DNA microarrays: a proof of principle study.

Journal of assisted reproduction and genetics - 1 Dec 2013

Altarescu G, Zeevi D A, Zeligson S, Perlberg S, Eldar-Geva T, Margalioth E J, Levy-Lahad E, Renbaum P

Abstract excerpt

PURPOSE: Development of PGD assays for molecular disorders is based on analysis of a familial mutation together with linked polymorphic STR markers; a process which is lengthy and requires the identification of multiple informative markers prior to PGD analysis. On the other hand, whole genome amplification (WGA), in conjunction with microarray platforms, allows the use of a universal assay for the analysis of a...

Read the complete abstract on PubMed

Topics

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

Share to Biopsy
Share to Charcot-Marie-Tooth Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Embryo Transfer

Share to Gene Amplification

Share to Genetic Diseases, Inborn

Share to Oligonucleotide Array Sequence Analysis

Share to Pregnancy

Share to Preimplantation Diagnosis

Source

Open in PubMed Open full text

Identifiers

PMID: 23832269
DOI: 10.1007/s10815-013-0044-8
PMCID: PMC3843181

Genes

PGD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Familial haplotyping and embryo analysis for Preimplantation genetic diagnosis (PGD) using DNA microarrays: a proof of principle study.PMID 23832269Read ↗

Proof of principle and first cases using preimplantation genetic haplotyping--a paradigm shift for embryo diagnosis.Semantic proximity Read ↗

Preimplantation genetic diagnosis guided by single-cell genomicsSemantic proximity Read ↗

Comprehensive preimplantation genetic testing by massively parallel sequencingSemantic proximity Read ↗

Preimplantation genetic haplotyping: 127 diagnostic cycles demonstrating a robust, efficient alternative to direct mutation testing on single cells.Semantic proximity Read ↗

A comprehensive and universal approach for embryo testing in patients with different genetic disorders.Semantic proximity Read ↗

PGD for hereditary breast and ovarian cancer: the route to universal tests for BRCA1 and BRCA2 mutation carriers.Semantic proximity Read ↗

Whole genome prediction for preimplantation genetic diagnosisSemantic proximity Read ↗

PGD for monogenic disorders: aspects of molecular biology.Semantic proximity Read ↗

Mutation and haplotype analysis for Duchenne muscular dystrophy by single cell multiple displacement amplification.Semantic proximity Read ↗

Single-cell high resolution melting analysis: A novel, generic, pre-implantation genetic diagnosis (PGD) method applied to cystic fibrosis (HRMA CF-PGD).Semantic proximity Read ↗

Clinical application of an Asian Screening Array-based preimplantation genetic testing workflow for various genetic disorders.Semantic proximity Read ↗

Pre-implantation genetic diagnosis for a family with Usher syndrome through targeted sequencing and haplotype analysisSemantic proximity Read ↗

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