Nomogram for estimating specific consanguinity risks
- PMID: 7108917
- PMCID: PMC1048869
- DOI: 10.1136/jmg.19.3.216
Nomogram for estimating specific consanguinity risks
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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