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Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA

✍ Scribed by Porreco, Richard P.; Garite, Thomas J.; Maurel, Kimberly; Marusiak, Barbara; Ehrich, Mathias; van den Boom, Dirk; Deciu, Cosmin; Bombard, Allan


Book ID
121662601
Publisher
Elsevier Science
Year
2014
Tongue
English
Weight
877 KB
Volume
211
Category
Article
ISSN
1097-6868

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