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PedAM

Pediatric Disease Annotations & Medicines




Disease lymphoid leukemia
Phenotype C0008625|chromosomal abnormality
Sentences 1
PubMedID- 20846384 Background: the hox11/tlx1 (hereafter referred to as hox11) homeobox gene was originally identified at a t(10;14)(q24;q11) translocation breakpoint, a chromosomal abnormality observed in 5-7% of t cell acute lymphoblastic leukemias (t-alls).

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