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Article

Noninvasive prenatal testing for 22q11.2 deletion syndrome: deeper sequencing increases the positive predictive value

6 Jun 2015

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Share to Fetal and Pediatric Neurological Disorders
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 25986033
DOI: 10.1016/j.ajog.2015.05.028

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Noninvasive prenatal testing for 22q11.2 deletion syndrome: deeper sequencing increases the positive predictive valuePMID 25986033Read ↗

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