Papiha S S, Bhattacharya S S, Roberts D F
Department of Human Genetics, University of Newcastle upon Tyne, UK.
Hum Hered. 1988;38(2):72-5. doi: 10.1159/000153761.
Restriction fragment length polymorphisms of the L1.28 probe which is closely linked to X-linked disorders, retinitis pigmentosa and Norrie disease, were studied in samples from England, India and Nigeria. The frequency of the A2 allele (9-kb fragment) was 0.23, 0.55 and 0.46 in England, India and Nigeria, respectively. The differences between the English and Indian populations were highly significant.
对与X连锁疾病、色素性视网膜炎和诺里病紧密连锁的L1.28探针的限制性片段长度多态性进行了研究,研究样本来自英格兰、印度和尼日利亚。在英格兰、印度和尼日利亚,A2等位基因(9千碱基片段)的频率分别为0.23、0.55和0.46。英格兰和印度人群之间的差异非常显著。