Morris M I, Hanson F W, Tennant F R
Department of Obstetrics and Gynecology, University of California, Davis, School of Medicine, Sacramento 95816.
Am J Obstet Gynecol. 1987 Oct;157(4 Pt 1):857-8. doi: 10.1016/s0002-9378(87)80071-6.
A novel Y/13 translocation was discovered in a female fetus during amniocentesis. The familial translocation is present in a phenotypically normal female sibling and in the father who also possesses a pericentric inversion. Karyotype of the father is 46,XY,-13,+der(13)t(Y;13)(q12;p12),inv(22)(p13q12.1).
在羊膜穿刺术期间,在一名女性胎儿中发现了一种新的Y/13易位。这种家族性易位存在于一名表型正常的女性同胞以及同样具有臂间倒位的父亲体内。父亲的核型为46,XY,-13,+der(13)t(Y;13)(q12;p12),inv(22)(p13q12.1)。