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Linkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16q24

Linkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16q24

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_69453548

Linkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16q24

About this item

Full title

Linkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16q24

Publisher

Cham: Springer International Publishing

Journal title

European journal of human genetics : EJHG, 2008-09, Vol.16 (9), p.1151-1154

Language

English

Formats

Publication information

Publisher

Cham: Springer International Publishing

More information

Scope and Contents

Contents

Infantile hypertrophic pyloric stenosis (IHPS) is the most common inherited form of gastrointestinal obstruction in infancy. The disease is considered a paradigm for the sex-modified model of multifactorial inheritance and affects males four times more frequently than females. However, extended pedigrees consistent with autosomal dominant inheritan...

Alternative Titles

Full title

Linkage of monogenic infantile hypertrophic pyloric stenosis to chromosome 16q24

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_69453548

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_69453548

Other Identifiers

ISSN

1018-4813

E-ISSN

1476-5438

DOI

10.1038/ejhg.2008.86

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