Hori T, Masuno M, Wakazono A, Takahashi E, Katakura R, Orii T
Division of Genetics, National Institute of Radiological Sciences, Chiba, Japan.
Jpn J Hum Genet. 1993 Jun;38(2):219-24. doi: 10.1007/BF01883713.
An interstitial deletion, del(11)(q14q22), found in a female infant was examined by fluorescence in situ hybridization with cosmid DNA markers mapped on the long arm of chromosome 11. Three cosmids mapped on 11q14.1-11q22.1 region were not hybridized to the del(11) chromosome, while all the other DNA markers mapped on 11cen-11q14.1 and 11q23.1-11qter region gave hybridization signals on the del(11) chromosome. Cytogenetic analysis after R-banding confirmed an apparent deletion of 11q14-q22, but containing a small R-negative band, a part of 11q22.3 and/or 11q14.1, in the middle part of del(11) chromosome. The karyotype thus was determined to be 46,XX,del(11)(q14.1q22.3).
在一名女婴中发现了一个间质性缺失del(11)(q14q22),利用定位在11号染色体长臂上的黏粒DNA标记,通过荧光原位杂交对其进行了检测。定位在11q14.1 - 11q22.1区域的三个黏粒未与del(11)染色体杂交,而定位在11cen - 11q14.1和11q23.1 - 11qter区域的所有其他DNA标记在del(11)染色体上均产生了杂交信号。R显带后的细胞遗传学分析证实了11q14 - q22存在明显缺失,但在del(11)染色体中部包含一条小的R阴性带,即11q22.3和/或11q14.1的一部分。因此,核型被确定为46,XX,del(11)(q14.1q22.3)。