Tomkins D J
Am J Hum Genet. 1981 Sep;33(5):745-51.
Unusual inheritance of a reciprocal translocation, t(11;22)(p11;p12)mat was discovered in a family with one daughter having a different translocation, t(11;15)(p11;p12). Another daughter inherited the same translocation as her mother. The breakpoints through the nucleolar organizing regions (NORs) of chromosomes 15 and 22 were determined by silver staining. A review of the literature has demonstrated that such unstable familial translocations are very rare and can occur either in mitosis or meiosis. They usually involve exchanges between centromeres, telomeres, or NORs.
在一个家庭中发现了一种罕见的相互易位遗传情况,即母亲为t(11;22)(p11;p12)的相互易位,其一个女儿却有不同的易位t(11;15)(p11;p12)。另一个女儿继承了与母亲相同的易位。通过银染确定了15号和22号染色体通过核仁组织区(NORs)的断点。文献综述表明,这种不稳定的家族性易位非常罕见,可发生在有丝分裂或减数分裂中。它们通常涉及着丝粒、端粒或NORs之间的交换。