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Nomogram for estimating specific consanguinity risks
  1. Ricardo Cruz-Coke
  1. Genetic Unit, Hospital J J Aguirre, and the Faculty of Medicine, University of Chile, Santiago, Chile

    Abstract

    This paper describes a nomogram to estimate the chance of consanguinity for specific autosomal recessive diseases, taking into account the gene frequencies (q) of the recessive alleles and the coefficient of inbreeding (F) of the family of the proband.

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