Neuroendocrine Tumors Are Enriched in Cowden Syndrome-Reference-Cited by-同舟云学术

Neuroendocrine Tumors Are Enriched in Cowden Syndrome

Published:2020-11 Issue:4 Volume: Page:551-556
ISSN:2473-4284
Container-title:JCO Precision Oncology
language:en
Short-container-title:JCO Precision Oncology

Author:

Greidinger Alison¹,Miller-Samuel Susan²,Giri Veda N.³⁴,Woo Michele Sue-Ann⁵,Akumalla Saranya⁵,Zeigler-Johnson Charnita⁶,Keith Scott W.⁷,Silver Daniel P.³

Affiliation:

1. Department of Medicine, Thomas Jefferson University, Philadelphia, PA

2. Cancer Risk Assessment and Clinical Cancer Genetics Program, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA

3. Department of Medical Oncology and Cancer Biology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, PA

4. Department of Urology, Thomas Jefferson University, Philadelphia, PA

5. Foundation Medicine, Cambridge, MA

6. Department of Medical Oncology, Thomas Jefferson University, Philadelphia, PA

7. Department of Pharmacology and Experimental Therapeutics, Division of Biostatistics, Thomas Jefferson University, Philadelphia, PA

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

Link

https://ascopubs.org/doi/pdfdirect/10.1200/PO.19.00241

Reference28 articles.

1. Novel PTEN mutations in patients with Cowden disease: absence of clear genotype–phenotype correlations

2. Cowden Syndrome and the PTEN Hamartoma Tumor Syndrome: Systematic Review and Revised Diagnostic Criteria

3. Will the real Cowden syndrome please stand up (again)? Expanding mutational and clinical spectra of the PTEN hamartoma tumour syndrome

4. Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing

5. A computational approach to distinguish somatic vs. germline origin of genomic alterations from deep sequencing of cancer specimens without a matched normal

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