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Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirs...

Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirs...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_71610762

Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease

About this item

Full title

Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease

Publisher

London: Elsevier Ltd

Journal title

The Lancet (British edition), 2002-04, Vol.359 (9313), p.1200-1205

Language

English

Formats

Publication information

Publisher

London: Elsevier Ltd

More information

Scope and Contents

Contents

Several genes, including the major susceptibility gene RET, have roles in development of Hirschsprung's disease. Results of genetic-linkage analysis of patients with familial disease with both long-segment and short-segment phenotypes have shown close linkage with the RET locus. We aimed to investigate whether both RET mutations and polymorphisms c...

Alternative Titles

Full title

Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_71610762

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_71610762

Other Identifiers

ISSN

0140-6736

E-ISSN

1474-547X

DOI

10.1016/S0140-6736(02)08218-1

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