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dc.contributor.authorTesoriero Aen
dc.contributor.authorVenter Den
dc.contributor.authorAndersen Cen
dc.contributor.authorSouthey Men
dc.contributor.authorSomers Gen
dc.contributor.authorMcKay Men
dc.contributor.authorArmes Jen
dc.contributor.authorMcCredie Men
dc.contributor.authorGiles Gen
dc.contributor.authorHopper JLen
dc.date.issued1999
dc.identifier.urihttps://hdl.handle.net/2123/30559
dc.publisherAmerican Journal of Human Geneticsen
dc.rightsOther
dc.subjectAllelesen
dc.subjectHumansen
dc.subjectLoss of Heterozygosityen
dc.subjectMaleen
dc.subjectMutationen
dc.subjectNeoplasm Proteinsen
dc.subjectPolymorphism,Geneticen
dc.subjectResearch Support,Non-U.S.Gov'ten
dc.subjectSequence Deletionen
dc.subjectTranscription Factorsen
dc.subjectBRCA2 Proteinen
dc.subjectbreasten
dc.subjectBreast Neoplasmsen
dc.subjectcanceren
dc.subjectFemaleen
dc.subjectGenes,Brca1en
dc.subjectgeneticsen
dc.subjectGerm-Line Mutationen
dc.subject.otherBiology – Cancer Progression and Metastasisen
dc.subject.otherCancer Type - Breast Canceren
dc.titleDe novo BRCA1 mutation in a patient with breast cancer and an inherited BRCA2 mutationen
dc.typeArticleen
usyd.facultyFaculty of Medicine and Health, The Daffodil Centreen


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