Multiplex genetic cancer testing identifies pathogenic mutations in TP53 and CDH1 in a patient with bilateral breast and endometrial adenocarcinoma

BACKGROUND: Germline genetic testing for familial cancer syndromes is usually performed serially for the most likely genetic causes. In recent years the way genetic testing carried out has changed, as next generation sequencing now allows the simultaneous testing of multiple susceptibility genes at...

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Detalles Bibliográficos
Autores principales: Heitzer, Ellen, Lax, Sigurd, Lafer, Ingrid, Müller, Stephanie M, Pristauz, Gunda, Ulz, Peter, Jahn, Stephan, Högenauer, Christoph, Petru, Edgar, Speicher, Michael R, Geigl, Jochen B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913615/
https://www.ncbi.nlm.nih.gov/pubmed/24373500
http://dx.doi.org/10.1186/1471-2350-14-129

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913615/
https://www.ncbi.nlm.nih.gov/pubmed/24373500
http://dx.doi.org/10.1186/1471-2350-14-129

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