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Single-step screening method for the most common mutations in familial adenomatous polyposis
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1993
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Genetic TestingMarion Mandl InstituteGeneticsGenetic EpidemiologyPathologyMolecular GeneticsDisease Gene IdentificationGenomicsGenetic MedicineClinical GeneticsGenetic AnalysisTranslational BiologyFamilial Adenomatous PolyposisCommon MutationsPublic HealthMolecular DiagnosticsMonogenic DisordersInherited Metabolic DiseaseSingle-step Screening MethodMolecular Diagnostic TechniquesGermany SearchGenetic DisorderMedical GeneticsD-53111 BonnMedicine
Journal Article Single-step screening method for the most common mutations in familial adenomatous polyposis Get access Waltraut Friedl, Waltraut Friedl * Institute for Humangenetik der UniversitatWithermstraBe 31, D-53111 Bonn, Germany * To whom correspondence should be addressed Search for other works by this author on: Oxford Academic PubMed Google Scholar Marion Mandl, Marion Mandl Institute for Humangenetik der UniversitatWithermstraBe 31, D-53111 Bonn, Germany Search for other works by this author on: Oxford Academic PubMed Google Scholar Marlies Sengteller Marlies Sengteller Institute for Humangenetik der UniversitatWithermstraBe 31, D-53111 Bonn, Germany Search for other works by this author on: Oxford Academic PubMed Google Scholar Human Molecular Genetics, Volume 2, Issue 9, September 1993, Pages 1481–1482, https://doi.org/10.1093/hmg/2.9.1481 Published: 01 September 1993 Article history Received: 19 April 1993 Revision received: 12 July 1993 Accepted: 12 July 1993 Published: 01 September 1993