Utilization of Mammalian Specific Locus Studies in Hazard Evaluation and Estimation of Genetic Risk 1983
DOI: 10.1007/978-1-4613-3739-3_6
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Biochemical Approaches to Monitoring Human Populations for Germinal Mutation rates: I. Electrophoresis

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Cited by 5 publications
(4 citation statements)
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“…This convention carries with it the risk of missing a mutation whose phenotype mimics a common polymorphism. Elsewhere we have calculated that the underestimation of mutation rates which results from this omission should be about 10% (Neel et al, 1983). On the other hand, undertaking a family investigation to test whether a common polymorphism was the result of a mutational event in a parent would have increased the work load of family studies by an order of magnitude basd on the actual polymorphism frequencies in these data.…”
Section: Discussionmentioning
confidence: 98%
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“…This convention carries with it the risk of missing a mutation whose phenotype mimics a common polymorphism. Elsewhere we have calculated that the underestimation of mutation rates which results from this omission should be about 10% (Neel et al, 1983). On the other hand, undertaking a family investigation to test whether a common polymorphism was the result of a mutational event in a parent would have increased the work load of family studies by an order of magnitude basd on the actual polymorphism frequencies in these data.…”
Section: Discussionmentioning
confidence: 98%
“…Blood samples were collected and processed as described by Neel et al (1979) and Fielek and Mohrenweiser (1979). An aliquot of cells was retained in a glycerol-sorbitol mixture for blood typing (Weiner and Lourie, 1981).…”
Section: Methodsmentioning
confidence: 99%
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