The 8p11 myeloproliferative syndrome owing to rare FGFR1OP2-FGFR1 fusion

European Journal of Haematology

Volumn 86, Issue 4, 2011, Pages 347-349

  Onozawa, Masahiro ^a   Ohmura, Kazumasa ^a   Ibata, Makoto ^a   Iwasaki, Junko ^a   Okada, Kohei ^a   Kasahara, Ikumi ^a   Yamaguchi, Keisuke ^a   Kubota, Kanako ^a   Fujisawa, Shinichi ^a   Shigematsu, Akio ^a   Endo, Tomoyuki ^a   Kondo, Takeshi ^a   Hashino, Satoshi ^a   Tanaka, Junji ^a   Matsuno, Yoshihiro ^a   Asaka, Masahiro ^a   Imamura, Masahiro ^a  

^a HOKKAIDO UNIVERSITY HOSPITAL   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR RECEPTOR 1;

ADULT; BONE MARROW BIOPSY; CASE REPORT; CHROMOSOME 8P; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; EOSINOPHILIA; FLUORESCENCE IN SITU HYBRIDIZATION; GENOME; HUMAN; LETTER; LYMPHADENOPATHY; MALE; MYELOPROLIFERATIVE DISORDER; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

ADULT; CHROMOSOME PAINTING; CHROMOSOMES, HUMAN, PAIR 12; CHROMOSOMES, HUMAN, PAIR 8; HUMANS; MALE; MYELOPROLIFERATIVE DISORDERS; ONCOGENE PROTEINS, FUSION; PROTO-ONCOGENE PROTEINS; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 1; SYNDROME; TRANSLOCATION, GENETIC;

EID: 79952741169     PISSN: 09024441     EISSN: 16000609     Source Type: Journal    
DOI: 10.1111/j.1600-0609.2010.01568.x     Document Type: Letter

References (5)

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