Sparkes R S, Salter W J, Blaker R G, Muller H M
Clin Genet. 1977 Aug;12(2):114-8. doi: 10.1111/j.1399-0004.1977.tb00912.x.
A baby boy with multiple congenital anomalies and low birth weight has an apparent de novo insertional translocation into the long arm of his only X chromosome. The origin of the translocated material is not evident and both cytogenetic and X-linked marker studies do not indicate any loss of genetic material from the X chromosome. His findings are compared with other males who have X-translocations, none of which appear to be insertional translocations.
一名患有多种先天性异常且出生体重低的男婴,其唯一的X染色体长臂上出现了明显的新发插入性易位。易位物质的来源不明确,细胞遗传学和X连锁标记研究均未表明X染色体有任何遗传物质丢失。将他的发现与其他患有X易位的男性进行了比较,这些人中没有一个是插入性易位。