Cannizzaro L A, Aronson M M, Emanuel B S
Cytogenet Cell Genet. 1985;39(3):173-8. doi: 10.1159/000132130.
Using a combination of banding techniques, we examined two atypical 21;22 translocations, 46,XX or XY,t(21;22)(p11;q11). In situ chromosomal hybridization of a probe for the constant region of the lambda light chain locus demonstrated that the 22q11 breakpoints of both rearrangements were proximal to the C lambda gene cluster. These studies permitted us to distinguish the 22q11 breakpoints of these translocations from the breakpoint of the 22q--chromosome of chronic myelogenous leukemia.
我们运用多种显带技术,检测了两例非典型的21;22易位,核型为46,XX或XY,t(21;22)(p11;q11)。用λ轻链基因座恒定区探针进行原位染色体杂交显示,两种重排的22q11断点均位于Cλ基因簇近端。这些研究使我们能够将这些易位的22q11断点与慢性粒细胞白血病22q-染色体的断点区分开来。