Concurrent myeloid sarcoma, atypical teratoid/rhabdoid tumor, and hypereosinophilia in an infant with a germline SMARCB1 mutation-Reference-Cited by-同舟云学术

Concurrent myeloid sarcoma, atypical teratoid/rhabdoid tumor, and hypereosinophilia in an infant with a germline SMARCB1 mutation

Published:2017-01-23 Issue:9 Volume:64 Page:e26460
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Metts Jonathan L.¹,Park Sunita I.²,Soares Bruno P.³,Fong Cindy⁴,Biegel Jaclyn A.⁴,Goldsmith Kelly C.¹

Affiliation:

1. Division of Hematology/Oncology; Department of Pediatrics, Aflac Cancer and Blood Disorders Center; Children's Healthcare of Atlanta and Emory University; Atlanta Georgia

2. Department of Pathology; Children's Healthcare of Atlanta and Emory University; Atlanta Georgia

3. Division of Pediatric Radiology and Pediatric Neuroradiology, Russell H. Morgan Department of Radiology and Radiological Science; The Johns Hopkins University School of Medicine; Baltimore Maryland

4. Department of Pathology and Laboratory Medicine, Children's Hospital Los Angeles and Keck School of Medicine, University of Southern California; Los Angeles California

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology, and Child Health

Reference13 articles.

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2. Update on pediatric cancer predisposition syndromes;Schiffman;Pediatr Blood Cancer,2013

3. Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors;Eaton;Pediatr Blood Cancer,2011

4. Frequent hSNF5/INI1 germline mutations in patients with rhabdoid tumor;Bourdeaut;Clin Cancer Res,2011

5. Expression of SMARCB1 (INI1) mutations in familial schwannomatosis;Smith;Hum Mol Genet,2012

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