A novel translocation t(10;17)(p13;q11.2) harboring two cryptic deletions identified by array‐CGH and characterized by SUZ12 overexpression in a patient with chronic thrombocytosis-Reference-Cited by-同舟云学术

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A novel translocation t(10;17)(p13;q11.2) harboring two cryptic deletions identified by array‐CGH and characterized by SUZ12 overexpression in a patient with chronic thrombocytosis

Published:2020-07-06 Issue:11 Volume:59 Page:661-666
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosomes Cancer

Author:

Batanian Jacqueline R.¹²,Malherbe Jacques A. J.³^ORCID,Erber Wendy N.³

Affiliation:

1. Department of Pediatrics SSM Cardinal Glennon Children's Hospital St. Louis MO USA

2. Department of Pathology St. Louis University School of Medicine, SSM Cardinal Glennon Children's Hospital St. Louis MO USA

3. School of Biomedical Sciences The University of Western Australia Crawley WA Australia

Publisher

Wiley

Subject

Cancer Research,Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/gcc.22881

Reference25 articles.

1. The 2016 WHO classification and diagnostic criteria for myeloproliferative neoplasms: document summary and in-depth discussion

2. Reproducibility of Histologic Classification in Nonfibrotic Myeloproliferative Neoplasia

3. Guideline for investigation and management of adults and children presenting with a thrombocytosis

4. Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis

5. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders

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