Rehder H, Brühl P, Seth P K
Urologe A. 1975 Jul;14(4):182-6.
A boy with XX-karyotype displayed classical features of Klinefelter's syndrome. In the nuclei of hair root cells Barr-bodies were present as well as brightly fluorescent (F-)bodies resembling closely a Y-body. In lymphocyte metaphases, however, this F-body of the interphase nuclei corresponded to a brightly fluorescent segment of the short arm of a D15-chromosome was found in the father's karyotype. This case does not give convincing support to any of the theories suggested in the etiology of the XX-male phenomenon.
一名具有XX核型的男孩表现出克兰费尔特综合征的典型特征。在发根细胞核中存在巴氏小体以及与Y小体极为相似的明亮荧光（F-）小体。然而，在淋巴细胞中期，间期细胞核中的这种F小体对应于父亲核型中一条D15染色体短臂上的一个明亮荧光片段。该病例并未为XX男性现象病因学中提出的任何理论提供令人信服的支持。
