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Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect

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Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_crossref_primary_10_1038_gim_2015_60

Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect

About this item

Full title

Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect

Author / Creator

D’Alessandro, Lisa C.A. , Al Turki, Saeed , Manickaraj, Ashok Kumar , Manase, Dorin , Mulder, Barbara J.M. , Bergin, Lynn , Rosenberg, Herschel C. , Mondal, Tapas , Gordon, Elaine , Lougheed, Jane , Smythe, John , Devriendt, Koen , Bhattacharya, Shoumo , Watkins, Hugh , Bentham, Jamie , Bowdin, Sarah , Hurles, Matthew E. and Mital, Seema

Journal title

Genetics in medicine, 2016-02, Vol.18 (2), p.189-198

Language

English

Formats

Articles

More information

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_crossref_primary_10_1038_gim_2015_60

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_crossref_primary_10_1038_gim_2015_60

Other Identifiers

ISSN

1098-3600

DOI

10.1038/gim.2015.60

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