Genetic heterogeneity in rhabdomyosarcoma revealed by SNP array analysis-Reference-Cited by-同舟云学术

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Genetic heterogeneity in rhabdomyosarcoma revealed by SNP array analysis

Published:2015-10-20 Issue:1 Volume:55 Page:3-15
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosomes Cancer

Author:

Walther Charles¹,Mayrhofer Markus²,Nilsson Jenny¹,Hofvander Jakob¹,Jonson Tord¹,Mandahl Nils¹,Øra Ingrid³,Gisselsson David¹,Mertens Fredrik¹

Affiliation:

1. Department of Clinical Genetics; University and Regional Laboratories, Skåne University Hospital, Lund University; Lund Sweden

2. Array & Analysis Facility, Science for Life Laboratory, Uppsala University; Sweden

3. Department of Pediatric Oncology; Skåne University Hospital; Lund Sweden

Funder

Swedish Childhood Cancer Foundation

Publisher

Wiley

Subject

Cancer Research,Genetics

Reference41 articles.

1. Recurrent MYOD1 mutations in pediatric and adult sclerosing and spindle cell rhabdomyosarcomas: Evidence for a common pathogenesis;Agaram;Genes Chromosomes Cancer,2014

2. Foxj3 transcriptionally activates Mef2c and regulates adult skeletal muscle fiber type identity;Alexander;Develop Biol,2010

3. Gene fusions involving PAX and FOX family members in alveolar rhabdomyosarcoma;Barr;Oncogene,2001

4. Genomic and clinical analyses of 2p24 and 12q13-q14 amplification in alveolar rhabdomyosarcoma: a report from the Children's Oncology Group;Barr;Genes Chromosomes Cancer,2009

5. SNP genotyping of a sclerosing rhabdomyosarcoma: Reveals highly anuploid profile and a specific MDM2/HMGA2 amplification;Bouron-Dal Soglio;Hum Pathol,2009

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