Bridge P J, Lillicrap D P
Department of Pathology, Kingston General Hospital, Ontario, Canada.
Am J Med Genet. 1989 May;33(1):92-9. doi: 10.1002/ajmg.1320330113.
We studied two small, two-generation families with the fragile X [Fra (X)] syndrome. The absolute phase of the DNA markers in relation to the disease in the mother was not known in either family. We present the derivation of risks for these families using flanking markers, taking into account the uncertainty regarding maternal phase. Since the use of flanking markers fails to yield useful counseling data in the 1/3 to 1/7 of all cases where a single recombination event occurs between the two flanking markers, we calculate the probability that this method is likely to be successful or unsuccessful when prenatal diagnosis is attempted using linked RFLPs.
我们研究了两个患有脆性X [Fra (X)] 综合征的小型两代家庭。在这两个家庭中,母亲体内DNA标记相对于疾病的绝对相位均未知。我们利用侧翼标记推导了这些家庭的风险,并考虑了母本相位的不确定性。由于在所有侧翼标记之间发生单次重组事件的1/3至1/7的病例中,使用侧翼标记无法得出有用的咨询数据,因此我们计算了在尝试使用连锁限制性片段长度多态性(RFLP)进行产前诊断时该方法可能成功或失败的概率。