| Literature DB >> 1355354 |
S Rand1, C Puers, K Skowasch, P Wiegand, B Budowle, B Brinkmann.
Abstract
Family studies were carried out in a population sample from north west Germany using 4 amplifiable VNTR polymorphic systems D1S80 (MCT118), ApoB, D17S30 (YNZ22) and COL2A1. Separation was carried out in polyacrylamide gels and visualised using silver staining. In family studies (n = 30) no evidence of new mutations was found. The population study of unrelated individuals (mothers and putative fathers) showed that all 4 systems were highly polymorphic and similar to other population studies. The combined exclusion chance was calculated to be approximately 99% and the combined discrimination index 1.5.10(-4). The Hardy-Weinberg equilibrium was checked by forming groups of alleles and no significant deviations could be found in all systems.Entities:
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Year: 1992 PMID: 1355354 DOI: 10.1007/bf01369552
Source DB: PubMed Journal: Int J Legal Med ISSN: 0937-9827 Impact factor: 2.686