Morton N E, Matsuura J, Bart R, Lew R
Clin Genet. 1978 Jun;13(6):449-61. doi: 10.1111/j.1399-0004.1978.tb01198.x.
By criterion scaling and principal component analysis of performance, social class, symptoms, institutionalization, and medical history, a cohort of mental defectives has been divided into medical, biological, and sociofamilial categories. This division, corresponding to differences in etiology and severity, reveals changing patterns of admission and provides evidence that male excess is not primarily due to sex linkage. The incidence of mental retardation increases about 5% with first-cousin marriage, in agreement with other studies. The decline of IQ with inbreeding appears to be due entirely to rare recessive genes, not to dominance deviations of polygenes.
通过对表现、社会阶层、症状、机构收容情况和病史进行标准缩放和主成分分析,一组智力缺陷者被分为医学、生物学和社会家庭类别。这种划分对应于病因和严重程度的差异,揭示了入院模式的变化,并提供证据表明男性比例过高并非主要由于性连锁。与其他研究一致,近亲结婚时智力迟钝的发生率增加约5%。近亲繁殖导致的智商下降似乎完全是由于罕见的隐性基因,而非多基因的显性偏差。