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https://www.readbyqxmd.com/read/24785862/noninvasive-prenatal-testing-for-microdeletion-syndromes-and-expanded-trisomies-proceed-with-caution
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Neeta L Vora, Barbara M O╩╝Brien
The identification of circulating cell-free fetal DNA in maternal plasma has led to the introduction of noninvasive prenatal tests with high sensitivity and high specificity for common aneuploidies (trisomy 13, trisomy 18, trisomy 21). A new expanded noninvasive prenatal testing panel that includes five microdeletion syndromes (22q11 deletion syndrome, cri-du-chat [5p minus], Prader Willi or Angelman syndrome, 1p36 deletion syndrome) and two aneuploidies usually associated with nonviable pregnancies (trisomy 16 and trisomy 22) is now available...
May 2014: Obstetrics and Gynecology
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