Sistonen P, Green C A, Lomas C G, Tippett P
Ann Hum Genet. 1983 Oct;47(4):277-84. doi: 10.1111/j.1469-1809.1983.tb00997.x.
Family studies of rare LW(a-b+) propositi confirm the recent finding based on frequency studies that the LW blood groups are polymorphic in Finland (Sistonen & Tippett, 1982); they are controlled by two alleles LWa (0.97) and LWb (0.03) independent from most other common blood group loci. Lod scores for LW and the loci for 27 markers are presented.
对罕见的LW(a-b+)个体的家系研究证实了基于频率研究的最新发现，即LW血型在芬兰具有多态性（西斯托宁和蒂皮特，1982年）；它们由两个等位基因LWa（0.97）和LWb（0.03）控制，这两个等位基因与大多数其他常见血型位点独立。文中给出了LW以及27个标记位点的连锁分析lod值。
