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dc.contributor.authorShaw-Smith, Charlesen
dc.date.accessioned2016-01-26T15:54:32Zen
dc.date.available2016-01-26T15:54:32Zen
dc.date.issued2015-12-11en
dc.identifier.citationMolecular Basis of Developmental Anomalies of the Human Gastrointestinal Tract 2015, 4 (1):1 Colloquium Series on Genomic and Molecular Medicineen
dc.identifier.issn2167-7840en
dc.identifier.issn2167-7859en
dc.identifier.doi10.4199/C00139ED1V01Y201509GMM006en
dc.identifier.urihttp://hdl.handle.net/11287/594899en
dc.description.abstractCurrent knowledge of the etiology of congenital malformations of the human gastrointestinal tract is covered in this book, prefaced by some introductory notes on embryological development. Malformations involving the esophagus, stomach, small and large intestine, anus and rectum, pancreas, and hepato-billiary system are covered. There is a focus on covering those malformations for which a molecular genetic etiology is understood, but other causations, including environmental exposures, twinning, and unknown etiology are also included. For completeness, some disorders are included which are not, strictly, malformations, or which do not, strictly, involve the gastrointestinal tract. Such disorders include Hirschsprung disease, congenital diaphragmatic hernia, omphalocele, and gastroschisis. Suggested approaches to clinical evaluation of individuals with gastrointestinal malformations are included.en
dc.language.isoenen
dc.publisherMorgan & Claypoolen
dc.relation.urlhttp://www.morganclaypool.com/doi/10.4199/C00139ED1V01Y201509GMM006en
dc.rightsArchived with thanks to Colloquium Series on Genomic and Molecular Medicine.en
dc.subjectWessex Classification Subject Headings::Gastroenterologyen
dc.titleMolecular Basis of Developmental Anomalies of the Human Gastrointestinal Tracten
dc.typeBooken
dc.identifier.journalColloquium Series on Genomic and Molecular Medicineen
dc.type.versionPublisheden


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