The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease
- Author
- KRATZ, Christian P; NIEMEYER, Charlotte M; STARY, Jan; TREBO, Monika; ZECCA, Marco; GELB, Bruce D; TARTAGLIA, Marco; LOH, Mignon L; CASTLEBERRY, Robert P; CETIN, Mualla; BERGSTRASSER, Eva; EMANUEL, Peter D; HASLE, Henrik; KARDOS, Gabriela; KLEIN, Cornelia; KOJIMA, Seiji
Department of Pediatric Hematology, Ihsan Dogramaci Children's Hospital, Hacettepe University, Ankara, Turkey
Department of Pediatric Hematology/Oncology and Division of Hematology/Oncology, Comprehensive Cancer Center, University of Alabama at Birmingham, AL, United States
Department of Pediatrics and Adolescent Medicine, University of Freiburg, Germany
Department of Pediatrics and the Comprehensive Cancer Center, University of California at San Francisco, CA, United States
Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan
Department of Pediatrics, Skejby Hospital, Aarhus University, Denmark
Department of Pediatrics, University Hospital Motol, Prague, Czech Republic
Department of Pediatrics, Zurich, Switzerland
Departments of Pediatrics and Human Genetics, Mount Sinai School of Medicine, New York, NY, United States
Dipartimento di Biologia Cellulare e Neuroscienze, Instituto Superiore di Sanità, Rome, Italy
Dutch Childhood Oncology Group, the Hague, Netherlands
Oncoernatologia Pediatrica, Instituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo, Pavia, Italy
St Anna Children's Hospital, Vienna, Austria - Source
Blood. 2005, Vol 106, Num 6, pp 2183-2185, 3 p ; ref : 30 ref
- ISSN
- 0006-4971
- Scientific domain
- Medical oncology; Hematology
- Publisher
- The Americain Society of Hematology, Washington, DC
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Génotype Génétique Homme Myéloprolifératif syndrome Noonan syndrome Phénotype Gène PTPN11 Leucémie myélomonocytaire juvénile Appareil circulatoire pathologie Hémopathie Maladie héréditaire Ostéochondrodysplasie Système nerveux pathologie Système ostéoarticulaire pathologie
- Keyword (en)
- Genotype Genetics Human Myeloproliferative syndrome Noonan syndrome Phenotype PTPN11 gene Juvenile myelomonocytic leukemia Cardiovascular disease Hemopathy Genetic disease Osteochondrodysplasia Nervous system diseases Diseases of the osteoarticular system
- Keyword (es)
- Genotipo Genética Hombre Mieloproliferativo síndrome Noonan síndrome Fenotipo Aparato circulatorio patología Hemopatía Enfermedad hereditaria Osteocondrodisplasia Sistema nervioso patología Sistema osteoarticular patología
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B15 Diseases of the osteoarticular system / 002B15H Malformations and congenital and or hereditary diseases involving bones. Joint deformations
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B19 Hematologic and hematopoietic diseases / 002B19B Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
- Discipline
- Blood diseases Osteoarticular pathology
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 17147373
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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DOI
10.1182/blood-2005-02-0531 
https://dx.doi.org/10.1182/blood-2005-02-0531
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