Morse H G, Hays T, Patterson D, Robinson A
Hum Genet. 1982;61(2):141-4. doi: 10.1007/BF00274204.
Use of the Giemsa-11 procedure for the localization of heterochromatic regions of human chromosomes and for differentiation of primate and rodent chromosomes has been somewhat limited since its discovery in 1972. An adaptation of this technique to the cytogenetic characterization of hematologic specimens has aided in the interpretation of translocations, deletions, and inversions involving human chromosome 9. The chromosomal analyses of 10% of over 100 patients, principally leukemic, were aided through the use of this auxiliary procedure. The diseases of these patients are given and portions of karyotypes are presented to show clarification of abnormalities made possible through the use of the Giemsa-11 technique.
自1972年发现以来,吉姆萨-11方法在定位人类染色体异染色质区域以及区分灵长类和啮齿类动物染色体方面的应用一直受到一定限制。将该技术应用于血液学标本的细胞遗传学特征分析,有助于解释涉及人类9号染色体的易位、缺失和倒位。通过使用这种辅助方法,对100多名主要为白血病患者中的10%进行了染色体分析,辅助了诊断。给出了这些患者的疾病情况,并展示了核型的部分内容,以显示通过吉姆萨-11技术能够明确异常情况。