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Newborn Sequencing in Genomic Medicine and Public Health.
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has minor subject area list
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Exome; Genetic Carrier Screening; Genetic Research; Genome-Wide Association Study; Genomic Structural Variation; Humans; Infant, Newborn; Intensive Care Units, Neonatal; Predictive Value of Tests; Prospective Studies; United States
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information resource reference
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Berg JS, Agrawal PB, Bailey DB, Beggs AH, Brenner SE, Brower AM, Cakici JA, Ceyhan-Birsoy O, Chan K, Chen F, Currier RJ, Dukhovny D, Green RC, Harris-Wai J, Holm IA, Iglesias B, Joseph G, Kingsmore SF, Koenig BA, Kwok PY, Lantos J, Leeder SJ, Lewis MA, McGuire AL, Milko LV, Mooney SD, Parad RB, Pereira S, Petrikin J, Powell BC, Powell CM, Puck JM, Rehm HL, Risch N, Roche M, Shieh JT, Veeraraghavan N, Watson MS, Willig L, Yu TW, Urv T, Wise AL. Newborn Sequencing in Genomic Medicine and Public Health. Pediatrics. 2017 Feb; 139(2).
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label
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Newborn Sequencing in Genomic Medicine and Public Health.
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