Sofuni T, Tanabe K, Naruto J, Awa A A
Humangenetik. 1975 Nov 6;30(2):91-7. doi: 10.1007/BF00291940.
Using chromosome banding techniques, a phenotypically normal male was found to have an abnormal banding pattern of the Y chromosome. By the constitutive heterochromatin staining method, a darkly stained band was located on the short arm and the proximal region of the long arm. The quinacrine staining method also showed a similar abnormal banding pattern: a brightly fluorescing band was seen on the short arm and the proximal region of the long arm. By the conventional Giemsa staining method, however, no specific morphological abnormality was detected in the aberrant Y. On detailed karyotype analyses no recognizable abnormality of banding patterns of any other chromosome was found aside from the abnormal Y. The abnormality was determined to be a complex inversion of the Y chromosome, which is described as 46,X,inv(Y)(pter leads to p11::q11 leads to q12::cen::q12 leads to qter).
运用染色体显带技术,发现一名表型正常的男性Y染色体具有异常的显带模式。通过组成型异染色质染色法,在短臂和长臂近端区域发现一条深色染色带。喹吖因染色法也显示出类似的异常显带模式:在短臂和长臂近端区域可见一条明亮荧光带。然而,通过传统吉姆萨染色法,在异常Y染色体上未检测到特定形态异常。在详细的核型分析中,除了异常的Y染色体外,未发现其他任何染色体的显带模式有可识别的异常。该异常被确定为Y染色体的复杂倒位,描述为46,X,inv(Y)(pter→p11::q11→q12::cen::q12→qter)。