Tetrasomy 21 transient leukemia with aGATA1 mutation in a phenotypically normal trisomy 21 mosaic infant: Case report and review of the literature
Claudio Sandoval(St. Jude Children's Research Hospital), Somasundaram Jayabose(New York Medical College), Sudha Sastry, Sharon R. Pine(University of Colorado Anschutz Medical Campus), David Kronn(New York Medical College), Qianxu Guo(New York Medical College), Julian M. Stewart(New York Medical College)
Cited by 25
Related Papers
The Notch signaling pathway as a mediator of tumor survival
|Carcinogenesis|2013|302
Schwannomatosis
|Neurology|1996|244
<i>MeCP2</i> mutations in children with and without the phenotype of Rett syndrome
|Neurology|2001|229
Secondary acute myeloid leukemia in children previously treated with alkylating agents, intercalating topoisomerase II inhibitors, and irradiation.
|Journal of Clinical Oncology|1993|191
Molecular Analysis of the NF2 Tumor-Suppressor Gene in Schwannomatosis
|The American Journal of Human Genetics|1997|184