©2011 Sequenom Center for Molecular Medicine.
Except for the historical information contained herein, the matters set forth in this press release, including statements regarding Sequenom's expected acceptance of samples and product launch and timing thereof for its RetnaGene™ AMD laboratory developed test, the expected publication of the manuscript "Clinical Validation of a Genetic Model to Estimate the Risk of Developing Choroidal Neovascular Age-related Macular Degeneration" in the June issue of Human Genomics, the expected use, application, impact, and the potential for improved patient care, associated with the RetnaGene™ AMD laboratory developed test, Sequenom's plans for exhibition and presentation at the 2011 Association for Research in Vision and Ophthalmology annual meeting, predictions regarding the number of cases of early AMD and late-stage blinding AMD in the future, Sequenom's commitment to improving healthcare through revolutionary genetic analysis solutions and dedication to development and commercialization of laboratory-developed genetic tests for prenatal and ophthalmic conditions, are forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. These forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially, including the risks and uncertainties associated with reliance upon the collaborative efforts of other parties, Sequenom's ability to develop and commercialize new technologies and products, particularly new technologies such as AMD, prenatal and other diagnostics and laboratory developed tests, Sequenom's ability to manage its existing cash resources or raise additional cash resources, competition, intellectual property protection and intellectual property rights of others, govern
|SOURCE Sequenom, Inc.|
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