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Volumn 92, Issue 11, 2007, Pages 1574-1575

Mutation analysis of the BRAF oncogene in juvenile myelomonocytic leukemia

Author keywords

BRAF; Juvenile myelomonocytic leukemia

Indexed keywords

ARTICLE; BRAF ONCOGENE; DISEASE ASSOCIATION; GENE IDENTIFICATION; GENE MUTATION; GENETIC SCREENING; HUMAN; JUVENILE MYELOMONOCYTIC LEUKEMIA; MAJOR CLINICAL STUDY; NEUROFIBROMATOSIS; ONCOGENE; SOMATIC MUTATION; TUMOR SUPPRESSOR GENE;

EID: 36348986709     PISSN: 03906078     EISSN: None     Source Type: Journal    
DOI: 10.3324/haematol.11493     Document Type: Article
Times cited : (13)

References (9)
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  • 2
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  • 3
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    • The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease
    • Kratz CP, Niemeyer CM, Castleberry RP, Cetin M, Bergstrasser E, Emanuel PD, et al. The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease. Blood 2005;106:2183-5.
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  • 4
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    • Mutations of the NF1 gene in children with juvenile myelomonocytic leukemia without clinical evidence of neurofibromatosis, type 1
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  • 8
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    • A pediatric approach to the WHO classification of myelodysplastic and myeloproliferative diseases
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  • 9
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    • Archambeault S, Yoshimi A, Kratz CP, Reising M, Fischer A, Noellke P, et al. Development of an allele-specific minimal residual disease assay for patients with Juvenile Myelomonocytic Leukemia-moving beyond clinical assessment. Blood 2006;108:[ASH Annual Meeting Abstracts].
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.