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Analysis of gene copy number variations in patients with congenital heart disease using multiplex li...

Analysis of gene copy number variations in patients with congenital heart disease using multiplex li...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6237800

Analysis of gene copy number variations in patients with congenital heart disease using multiplex ligation-dependent probe amplification

About this item

Full title

Analysis of gene copy number variations in patients with congenital heart disease using multiplex ligation-dependent probe amplification

Publisher

Turkey: Kare Publishing

Journal title

Anatolian journal of cardiology, 2018-07, Vol.20 (1), p.9-15

Language

English

Formats

Publication information

Publisher

Turkey: Kare Publishing

Subjects

Subjects and topics

More information

Scope and Contents

Contents

At the molecular and cellular levels, heart development entails the precise orchestration of genetic events such as the interplay of master transcriptional regulators, signaling pathways, and chromatin remodeling. Recent studies among patients with congenital heart disease (CHD) have shown the importance of recurrent copy number variations (CNVs) i...

Alternative Titles

Full title

Analysis of gene copy number variations in patients with congenital heart disease using multiplex ligation-dependent probe amplification

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6237800

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6237800

Other Identifiers

ISSN

2149-2263

E-ISSN

2149-2271

DOI

10.14744/AnatolJCardiol.2018.70481

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