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Anaplastic Rhabdomyosarcoma in TP53 Germline Mutation Carriers

Author
HETTMER, Simone1 2 3 4 ; ARCHER, Natasha M1 ; SOMERS, Gino R5 6 ; NOVOKMET, Ana7 ; WAGERS, Amy J3 4 ; DILLER, Lisa1 2 ; RODRIGUEZ-GALINDO, Carlos1 2 ; TEOT, Lisa A8 ; MALKIN, David7
[1] Department of Pediatric Oncology, Dana-Farber Cancer Institute and Division of Pediatric Hematology/ Oncology, Boston Children's Hospital, Boston, Massachusetts, United States
[2] Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, United States
[3] Howard Hughes Medical Institute, Department of Stem Cell and Regenerative Biology, Harvard University, Harvard Stem Cell Institute, Cambridge, Massachusetts, United States
[4] Joslin Diabetes Center, Boston, Massachusetts, United States
[5] Department of Pediatric Laboratory Medicine, The Hospital for Sick Children, University of Toronto, Toronto, Canada
[6] Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Canada
[7] Division of Oncology, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, Canada
[8] Department of Pathology, Boston Children's Hospital, Boston, Massachusetts, United States
Source

Cancer. 2014, Vol 120, Num 7, pp 1068-1075, 8 p ; ref : 44 ref

CODEN
CANCAR
ISSN
0008-543X
Scientific domain
Medical oncology
Publisher
Wiley-Blackwell, Hoboken, NJ
Publication country
United States
Document type
Article
Language
English
Author keyword
Li-Fraumeni syndrome TP53 anaplasia germline mutations rhabdomyosarcoma
Keyword (fr)
Cancérologie Gène TP53 Gène suppresseur tumeur Génétique Lignée germinale Mutation Porteur Rhabdomyosarcome Sarcome des tissus mous Syndrome de Li-Fraumeni Anaplasie Cancer Maladie héréditaire Multiple Pathologie du muscle strié Tumeur maligne
Keyword (en)
Cancerology TP53 Gene Tumor suppressor gene Genetics Germ line Mutation Carrier Rhabdomyosarcoma Soft tissue sarcoma Li-Fraumeni syndrome Cancer Genetic disease Multiple Striated muscle disease Malignant tumor
Keyword (es)
Cancerología Gen TP53 Gen supresor tumor Genética Línea germinal Mutación Portador Rabdomiosarcoma Sarcoma de tejidos blandos Li-Fraumeni síndrome Cáncer Enfermedad hereditaria Múltiple Músculo estriado patología Tumor maligno
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B04 Tumors / 002B04C Multiple tumors. Solid tumors. Tumors in childhood (general aspects)

Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B15 Diseases of the osteoarticular system / 002B15C Tumors of striated muscle and skeleton

Discipline
Osteoarticular pathology Tumours
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
28319730

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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