Population screening for carrier status: Effects of test limitations on precision of carrier prevalence rates
Author:
Publisher
Wiley
Subject
Genetics(clinical)
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1. Carrier Frequency of the Common Mutation IVS8-1G>C in DHCR7 and Estimate of the Expected Incidence of Smith–Lemli–Opitz Syndrome;Molecular Genetics and Metabolism;2001-01
2. Heterozygosity for the Common LCHAD Mutation (1528G>C) Is Not a Major Cause of HELLP Syndrome and the Prevalence of the Mutation in the Dutch Population Is Low;Pediatric Research;2000-08
3. Population-Based Estimates of Surfactant Protein B Deficiency;Pediatrics;2000-03-01
4. The incidence of cystic fibrosis in Scotland calculated from heterozygote frequencies;Clinical Genetics;1998-01
5. Prevalence of carriers of the most common medium-chain acyl-CoA dehydrogenase (MCAD) deficiency mutation (G985A) in The Netherlands;Human Genetics;1996-05-30
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