High‐resolution genomic analysis suggests the absence of recurrent genomic alterations other than SMARCB1 aberrations in atypical teratoid/rhabdoid tumors-Reference-Cited by-同舟云学术

High‐resolution genomic analysis suggests the absence of recurrent genomic alterations other than SMARCB1 aberrations in atypical teratoid/rhabdoid tumors

Published:2012-10-17 Issue:2 Volume:52 Page:185-190
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosom. Cancer

Author:

Hasselblatt Martin¹,Isken Sarah¹,Linge Anna¹,Eikmeier Kristin¹,Jeibmann Astrid¹,Oyen Florian²,Nagel Inga³⁴,Richter Julia³⁴,Bartelheim Kerstin⁵,Kordes Uwe²,Schneppenheim Reinhard²,Frühwald Michael⁵⁶,Siebert Reiner³,Paulus Werner¹

Affiliation:

1. Institute of Neuropathology, University Hospital Münster, Münster, Germany

2. Department of Pediatric Hematology and Oncology, University Medical Center Hamburg‐Eppendorf, Hamburg, Germany

3. Institute of Human Genetics, Christian‐Albrechts University Kiel, Kiel, Germany

4. Institute of Human Genetics, University Hospital Schleswig‐Holstein, Kiel, Germany

5. Department of Pediatric Hematology and Oncology, Klinikum Augsburg, Augsburg, Germany

6. Department of Pediatric Hematology and Oncology, University Hospital Münster, Münster, Germany

Publisher

Wiley

Subject

Cancer Research,Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/gcc.22018

Reference18 articles.

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2. Claudin-6 is of Limited Sensitivity and Specificity for the Diagnosis of Atypical Teratoid/Rhabdoid Tumors

3. Alterations of the hSNF5/INI1 gene in central nervous system atypical teratoid/rhabdoid tumors and renal and extrarenal rhabdoid tumors;Biegel JA;Clin Cancer Res,2002

4. Claudin 6 Is a Positive Marker for Atypical Teratoid/Rhabdoid Tumors

5. Clinicopathologic prognostic factors in childhood atypical teratoid and rhabdoid tumor of the central nervous system

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