A new PTPN11 mutation in juvenile myelomonocytic leukaemia associated with Noonan syndrome

被引：5

作者：

Giovannini, L

Cavé, H

Ferrero-Vacher, C

Boutte, P

Sirvent, N

机构：

[1] CHU Nice, Hop Archet, Serv Pediat, F-06202 Nice, France

[2] Hop Robert Debre, Biochim Genet Lab, AP HP, F-75019 Paris, France

[3] CHU Nice, Hop Archet, Cent Hematol Lab, F-06202 Nice, France

来源：

ACTA PAEDIATRICA | 2005年 / 94卷 / 05期

关键词：

D O I：

10.1080/08035250510027264

中图分类号：

R72 [儿科学];

学科分类号：

100202 [儿科学];

摘要：

引用

页码：636 / 637

页数：2

共 6 条

[1]

A pediatric approach to the WHO classification of myelodysplastic and myeloproliferative diseases [J].

Hasle, H ;

Niemeyer, CM ;

Chessells, JM ;

Baumann, I ;

Bennett, JM ;

Kerndrup, G ;

Head, DR .

LEUKEMIA, 2003, 17 (02) :277-282

[2]

Mutations in PTPN11 implicate the SHP-2 phosphatase in leukemogenesis [J].

Loh, ML ;

Vattikuti, S ;

Schubbert, S ;

Reynolds, MG ;

Carlson, E ;

Lieuw, KH ;

Cheng, JW ;

Lee, CM ;

Stokoe, D ;

Bonifas, JM ;

Curtiss, NP ;

Gotlib, J ;

Meshinchi, S ;

Le Beau, MM ;

Emanuel, PD ;

Shannon, KM .

BLOOD, 2004, 103 (06) :2325-2331

[3]

Transient abnormal myelopoiesis in Noonan syndrome [J].

Silvio, F ;

Carlo, L ;

Elena, B ;

Nicoletta, B ;

Daniela, F ;

Roberto, M .

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2002, 24 (09) :763-764

[4]

SHP-2 and myeloid malignancies [J].

Tartaglia, M ;

Niemeyer, CM ;

Shannon, KM ;

Loh, ML .

CURRENT OPINION IN HEMATOLOGY, 2004, 11 (01) :44-50

[5]

Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia [J].

Tartaglia, M ;

Niemeyer, CM ;

Fragale, A ;

Song, XL ;

Buechner, J ;

Jung, A ;

Hählen, K ;

Hasle, H ;

Licht, JD ;

Gelb, BD .

NATURE GENETICS, 2003, 34 (02) :148-150

[6]

PTPN11 mutations in Noonan syndrome:: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity [J].

Tartaglia, M ;

Kalidas, K ;

Shaw, A ;

Song, XL ;

Musat, DL ;

van der Burgt, I ;

Brunner, HG ;

Bertola, DR ;

Crosby, A ;

Ion, A ;

Kucherlapati, RS ;

Jeffery, S ;

Patton, MA ;

Gelb, BD .

AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (06) :1555-1563

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