Chronic myelomonocytic leukemia in childhood: A retrospective analysis of 110 cases. European Working Group on Myelodysplastic Syndromes in Childhood (EWOG-MDS)
C.M. Niemeyer, M. Arico, G. Basso, A. Biondi, A. Cantu Rajnoldi, U. Creutzig, and et al. Chronic myelomonocytic leukemia in childhood: a retrospective analysis of 110 cases. European Working Group on Myelodysplastic Syndromes in Childhood (EWOG-MDS) Blood 89 1997 3534 3543
Juvenile myelomonocytic leukemia: A report from the 2nd International JMML Symposium
R.J. Chan, T. Cooper, C.P. Kratz, B. Weiss, and M.L. Loh Juvenile myelomonocytic leukemia: a report from the 2nd International JMML Symposium Leuk Res 33 2009 355 362
Juvenile myelomonocytic leukemia: Report of seven cases and review of literature
L. Urs, S.J. Qualman, and S.B. Kahwash Juvenile myelomonocytic leukemia: report of seven cases and review of literature Pediatr Dev Pathol 12 2009 136 142
Transient myeloproliferation mimicking JMML associated with parvovirus infection of infancy
N. Gupta, R. Gupta, and S. Bakhshi Transient myeloproliferation mimicking JMML associated with parvovirus infection of infancy Pediatr Blood Cancer 52 2009 411 413
Diagnosing myelodysplastic/myeloproliferative neoplasms: Laboratory testing strategies to exclude other disorders
J. Hall, and K. Foucar Diagnosing myelodysplastic/myeloproliferative neoplasms: laboratory testing strategies to exclude other disorders Int J Lab Hematol 32 2010 559 571
A 3-bp deletion mutation of PTPN11 in an infant with severe Noonan syndrome including hydrops fetalis and juvenile myelomonocytic leukemia
R. Yoshida, M. Miyata, T. Nagai, T. Yamazaki, and T. Ogata A 3-bp deletion mutation of PTPN11 in an infant with severe Noonan syndrome including hydrops fetalis and juvenile myelomonocytic leukemia Am J Med Genet A 128A 2004 63 66
Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
M. Tartaglia, E.L. Mehler, R. Goldberg, G. Zampino, H.G. Brunner, H. Kremer, and et al. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome Nat Genet 29 2001 465 468