Guanti G, Mollica G, Polimeno L, Maritato F
Hum Genet. 1976 Jul 27;33(2):103-7. doi: 10.1007/BF00281883.
A malformed female infant was found to have a 46,XX complement with a chromosome 8 shorter than normal with a secondary constriction and satellites on the short arm. Chromosome studies on the clinically normal father showed a balanced translocation between chromosome 8 and 13, i.e., 46,XY,t(8;13) (p21 p12). The proposita, carrier of the unbalanced form of the translocation, resulted partially monosomic for short arm of chromosome 8 (8p-) and partially trisomic for short arm of chromosome 13. The levels of DNA complementary to rRNA (normal in the father who had 10 NOR and increased in the proposita who had 11 NOR) confirmed our interpretation of the rearrangement.
一名畸形女婴被发现其染色体组型为46,XX,其中一条8号染色体比正常的短,短臂上有次缢痕和随体。对临床正常的父亲进行的染色体研究显示,8号染色体与13号染色体之间存在平衡易位,即46,XY,t(8;13) (p21 p12)。先证者是这种易位不平衡形式的携带者,导致8号染色体短臂部分单体性(8p-)和13号染色体短臂部分三体性。与rRNA互补的DNA水平(在有10个核仁组织区的父亲中正常,在有11个核仁组织区的先证者中升高)证实了我们对这种重排的解释。