Incidental detection of germline variants of potential clinical significance by massively parallel sequencing in haematological malignancies.

Yannakou, Costas K; Jones, Kate; Ryland, Georgina L; Thompson, Ella R; Reid, Gareth; McBean, Michelle; Trainer, Alison; Westerman, David; Blombery, Piers

Yannakou, Costas K; Jones, Kate; Ryland, Georgina L; Thompson, Ella R; Reid, Gareth; McBean, Michelle; Trainer, Alison; Westerman, David; Blombery, Piers.

Affiliation

Yannakou CK; Peter MacCallum Cancer Centre, Melbourne, Australia.
Jones K; University of Melbourne, Melbourne, Australia.
Ryland GL; Peter MacCallum Cancer Centre, Melbourne, Australia.
Thompson ER; Peter MacCallum Cancer Centre, Melbourne, Australia.
Reid G; Peter MacCallum Cancer Centre, Melbourne, Australia.
McBean M; University of Melbourne, Melbourne, Australia.
Trainer A; Peter MacCallum Cancer Centre, Melbourne, Australia.
Westerman D; Peter MacCallum Cancer Centre, Melbourne, Australia.
Blombery P; Peter MacCallum Cancer Centre, Melbourne, Australia.

J Clin Pathol ; 71(1): 84-87, 2018 Jan.

Article in En | MEDLINE | ID: mdl-28801348

Subject(s)

Biomarkers, Tumor/genetics; Hematologic Neoplasms/genetics; High-Throughput Nucleotide Sequencing/methods; Neoplasms/genetics; Germ-Line Mutation; Hematologic Neoplasms/diagnosis; Humans

Key words

cancer genetics; haemato-oncology; haematopathology; inherited pathology

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers, Tumor / Hematologic Neoplasms / High-Throughput Nucleotide Sequencing / Neoplasms Type of study: Diagnostic_studies / Prognostic_studies Limits: Humans Language: En Journal: J Clin Pathol Year: 2018 Document type: Article Affiliation country: Australia Country of publication: United kingdom

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