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Ambry Genetics Introduces AmbryScreen(TM), a Genetic Test Screening for Some of the Most Common and Severe Genetic Disorders Affecting Newborns.
Date:5/17/2010

SAN FRANCISCO, May 17 /PRNewswire/ -- Ambry Genetics announced today at the American College of Obstetricians and Gynecologists annual clinical meeting the launch of AmbryScreen™, a genetic screening test used to identify carriers of some of the most severe and common childhood diseases affecting pan-ethnic populations.  Designed by a team of geneticists and genetic counselors with decades of clinical and laboratory experience, the panel is a responsible and ethical means of identifying individuals at high risks to have a child with severe genetic conditions.  As with all clinical assays performed by Ambry Genetics, the test must be ordered by a physician.  It is not available direct to consumer.

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The AmbryScreen™ test screens for over 90 childhood onset conditions representing only severe or common diseases. The core of the AmbryScreen™ test is the most sensitive Cystic Fibrosis carrier mutation panel in the marketplace.  It was designed by coupling the public databases of information along with Ambry's extensive database of over 25,000 patients sequenced in the last decade.  Our 100 CF mutation panel includes only well defined disease causing mutations, without containing mild CF mutations like some competing tests.  

"Ambry Genetics was founded on the idea of a comprehensive carrier test and now new technologies have enabled us to create a test that makes sense for patients and for physicians.  When we saw other companies launch seriously flawed tests, the team of Ambry genetic counselors set out to design a superior test.
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SOURCE Ambry Genetics
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