Wolstenholme J, Faed M J, Robertson J, Lamont M A
Hum Genet. 1983;63(1):45-7. doi: 10.1007/BF00285396.
A series of couples with histories of recurrent abortions and in whom one partner had been shown to have a major chromosomal anomaly were investigated with respect to the karyotypes of conceptions subsequent to ascertainment. The reproductive histories of translocation carriers amongst relatives were also studied. Results were compatible with previous reports of the behaviour of translocation chromosomes at meiosis with an additional previously undescribed outcome as a result of a maternal 13/14 Robertsonian translocation.
对一系列有反复流产史且一方被证明有主要染色体异常的夫妇进行了研究，以确定确诊后妊娠的核型。还研究了亲属中易位携带者的生殖史。结果与先前关于减数分裂时易位染色体行为的报道一致，并且由于母源性13/14罗伯逊易位出现了一个先前未描述的额外结果。
