Literature DB >> 3858219

Multiallelic restriction fragment polymorphisms in genetic counseling: population genetic considerations.

M A Asmussen, M T Clegg.   

Abstract

The use of selectively neutral, multiallelic molecular markers to trace the transmission of tightly linked genes is examined theoretically for all genetic counseling situations in which the diagnosis of deleterious progeny is desired. Formulae are computed in terms of the gametic frequency distribution in the population, for the expected fraction of matings (alpha i) which allow exact diagnosis on the basis of the marker alleles transmitted, assuming an arbitrary number (n) of alleles segregating at the marker locus and possibly nonrandom associations between the loci. In each case, it is shown that the diagnostic value of a multiallelic marker increases as n increases, with approximately 1-1/n matings informative, on average.

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Year:  1985        PMID: 3858219     DOI: 10.1159/000153533

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  1 in total

1.  Detection of DNA sequence polymorphisms by enzymatic amplification and direct genomic sequencing.

Authors:  D W Yandell; T P Dryja
Journal:  Am J Hum Genet       Date:  1989-10       Impact factor: 11.025

  1 in total

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