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Gene identification using exon amplification on human chromosome 18q21: implications for bipolar dis...

Gene identification using exon amplification on human chromosome 18q21: implications for bipolar dis...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_72328983

Gene identification using exon amplification on human chromosome 18q21: implications for bipolar disorder

About this item

Full title

Gene identification using exon amplification on human chromosome 18q21: implications for bipolar disorder

Publisher

Basingstoke: Nature Publishing Group

Journal title

Molecular psychiatry, 2000-09, Vol.5 (5), p.502-509

Language

English

Formats

Publication information

Publisher

Basingstoke: Nature Publishing Group

More information

Scope and Contents

Contents

We previously reported linkage between bipolar disorder and a region on human chromosome (HC) 18q21. To identify genes in this region, exon trapping was performed on cosmids isolated from an HC18-specific cosmid library (LL18NC02) using 47 sequence tagged site (STS) markers from 18q21 as hybridization probes. A total of 285 unique sequences (exons)...

Alternative Titles

Full title

Gene identification using exon amplification on human chromosome 18q21: implications for bipolar disorder

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_72328983

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_72328983

Other Identifiers

ISSN

1359-4184

E-ISSN

1476-5578

DOI

10.1038/sj.mp.4000780

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