Sandkuyl L, Ott J
Department of Psychiatry, Columbia University, New York, NY 10032.
Hum Genet. 1989 May;82(2):159-62. doi: 10.1007/BF00284050.
For the situation of a Mendelian disease linked to a genetic marker, a new method is described that allows evaluating for genetic counseling the information potentially available from the linked marker before the marker data are actually obtained, that is, prior to drawing blood for marker typing. For a consultand in a family pedigree, the method determines the risk distribution (small families) or an approximation to it (larger families) and calculates the probability that the risk will deviate beyond certain limits from its a priori value, which exists without marker data, for example, that the risk will be smaller than 0.10 or larger than 0.90. The method was applied here to a pedigree of 15 individuals for which analytical calculations would be difficult to carry out.
对于与遗传标记相关的孟德尔疾病情况,本文描述了一种新方法,该方法能够在实际获取标记数据之前,即在采集血液进行标记分型之前,评估从连锁标记中潜在可获得的信息,以用于遗传咨询。对于家系中的咨询者,该方法确定风险分布(小家系)或其近似值(大家系),并计算风险偏离其无标记数据时的先验值超过特定限度的概率,例如,风险小于0.10或大于0.90的概率。本文将该方法应用于一个有15个个体的家系,对于该家系进行分析计算会很困难。