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HerediT CF provider sheet

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WHICH CF MUTATIONS CAUSE DISEASE? Our team at Sequenom Laboratories has kept up with these changes with our HerediT Cystic Fibrosis carrier screening laboratory-developed test. We have updated our panel, bringing the most recent interpretations of the CFTR gene to you and your patients, based on the renowned Johns Hopkins CFTR2 database. The CFTR2 database has amassed the largest collection of phenotypic and CFTR gene function data available. Using patient registries in 24 countries, information on nearly 40,000 of the approximate 70,000 world-wide patients with cystic fibrosis (CF) has been cataloged. Mutations known to be associated with the cystic fibrosis gene (CFTR) have changed greatly since the gene was discovered in 1989. Has your CF mutation panel kept up with the changes? CHANGE YOUR CF TEST. FOR GOOD. THE HEREDIT CYSTIC FIBROSIS CARRIER SCREENING TEST. MUTATIONS THAT MATTER. The Clinical and Functional TRanslation of CFTR (CFTR2); available at http://cftr2.org. It has amassed the largest collection of phenotypic and CFTR gene function data available. Cystic Fibrosis Carrier Screening laboratory-developed test

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