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SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unb...

SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unb...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3421116

SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unbalanced translocations

About this item

Full title

SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unbalanced translocations

Publisher

Basingstoke: Nature Publishing Group

Journal title

European journal of human genetics : EJHG, 2012-09, Vol.20 (9), p.938-944

Language

English

Formats

Publication information

Publisher

Basingstoke: Nature Publishing Group

More information

Scope and Contents

Contents

Preimplantation genetic diagnosis (PGD) for chromosomal rearrangements (CR) is mainly based on fluorescence in situ hybridisation (FISH). Application of this technique is limited by the number of available fluorochromes, the extensive preclinical work-up and technical and interpretative artefacts. We aimed to develop a universal, off-the-shelf prot...

Alternative Titles

Full title

SNP array-based copy number and genotype analyses for preimplantation genetic diagnosis of human unbalanced translocations

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3421116

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3421116

Other Identifiers

ISSN

1018-4813

E-ISSN

1476-5438

DOI

10.1038/ejhg.2012.27

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