Cystic Fibrosis Carrier Screening: Steps in the Development of a Mutation Panel
Author:
Affiliation:
1. Genetics/Pediatrics, Weill Medical College of Cornell University, New York, NY 10021
Publisher
Mary Ann Liebert Inc
Subject
Genetics (clinical)
Link
http://www.liebertpub.com/doi/pdf/10.1089/10906570152742272
Reference22 articles.
1. High heterogeneity for cystic fibrosis in Spanish families: 75 mutations account for 90% of chromosomes
2. Detection of Five Rare Cystic Fibrosis Mutations Peculiar to Southern Italy: Implications in Screening for the Disease and Phenotype Characterization for Patients with Homozygote Mutations
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