The First Korean Case of Childhood Acute Myeloid Leukemia with Inv(11)(p15q22)/NUP98-DDX10 Rearrangement: A Rare but Recurrent Genetic Abnormality.
10.3343/alm.2014.34.6.478
- Author:
Rihwa CHOI
1
;
Mi Ae JANG
;
Keon Hee YOO
;
Seung Tae LEE
;
Hee Jin KIM
;
Sun Hee KIM
Author Information
1. Department of Laboratory Medicine & Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. sunnyhk@skku.edu
- Publication Type:Case Reports ; Letter
- MeSH:
Asian Continental Ancestry Group/*genetics;
Base Sequence;
Bone Marrow Cells/metabolism/pathology;
Child, Preschool;
Chromosome Inversion/*genetics;
*Chromosomes, Human, Pair 11;
DEAD-box RNA Helicases/*genetics;
Humans;
Karyotyping;
Leukemia, Myeloid, Acute/*diagnosis/genetics;
Male;
Nuclear Pore Complex Proteins/*genetics;
Republic of Korea
- From:Annals of Laboratory Medicine
2014;34(6):478-480
- CountryRepublic of Korea
- Language:English
-
Abstract:
No abstract available.
