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Embryo genome profiling by single-cell sequencing for preimplantation genetic diagnosis in a β-thala...

Embryo genome profiling by single-cell sequencing for preimplantation genetic diagnosis in a β-thala...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1667964910

Embryo genome profiling by single-cell sequencing for preimplantation genetic diagnosis in a β-thalassemia family

About this item

Full title

Embryo genome profiling by single-cell sequencing for preimplantation genetic diagnosis in a β-thalassemia family

Publisher

England

Journal title

Clinical chemistry (Baltimore, Md.), 2015-04, Vol.61 (4), p.617-626

Language

English

Formats

Publication information

Publisher

England

More information

Scope and Contents

Contents

The embryonic genome, including genotypes and haplotypes, contains all the information for preimplantation genetic diagnosis, representing great potential for mendelian disorder carriers to conceive healthy babies.
We developed a strategy to obtain the full embryonic genome for a β-thalassemia-carrier couple to have a healthy second baby. We car...

Alternative Titles

Full title

Embryo genome profiling by single-cell sequencing for preimplantation genetic diagnosis in a β-thalassemia family

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_1667964910

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1667964910

Other Identifiers

ISSN

0009-9147

E-ISSN

1530-8561

DOI

10.1373/clinchem.2014.228569

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