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The Journal of Pediatrics|April 16, 2008
Neonatal vitamin B12 deficiency secondary to maternal subclinical pernicious anemia: identification by expanded newborn screeningMichael Marble, Sara Copeland, Nashat Khanfar, et al.
Developmental Disabilities Research Reviews|July 23, 2008
Feeding and swallowing dysfunction in genetic syndromesLinda Cooper-Brown, Sara Copeland, Scott Dailey, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|April 5, 2013
The influence of maternal disease on metabolites measured as part of newborn screeningKelli K Ryckman, Oleg A Shchelochkov, Daniel E Cook, et al.
AMIA ... Annual Symposium Proceedings. AMIA Symposium|February 25, 2011
Standardizing newborn screening results for health information exchangeSwapna Abhyankar, Michele A Lloyd-Puryear, Rebecca Goodwin, et al.
American Journal of Medical Genetics. Part A|October 2, 2012
2q24 deletions: further characterization of clinical findings and their relation to the SCN clusterManjunath Nimmakayalu, Nathan Noble, V Kim Horton, et al.
International Journal of Neonatal Screening|June 5, 2018
Case Definitions for Conditions Identified by Newborn Screening Public Health SurveillanceMarci K Sontag, Deboshree Sarkar, Anne M Comeau, et al.
Molecular Genetics and Metabolism|January 14, 2009
High-frequency detection of deletions and variable rearrangements at the ornithine transcarbamylase (OTC) locus by oligonucleotide array CGHOleg A Shchelochkov, Fang-Yuan Li, Michael T Geraghty, et al.
Maternal and Child Health Journal|October 9, 2013
Evaluation of a novel electronic genetic screening and clinical decision support tool in prenatal clinical settingsEmily A Edelman, Bruce K Lin, Teresa Doksum, et al.
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