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Year | Number of Results |
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2012 | 1 |
2022 | 2 |
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Page 1
Newborn screening for mucopolysaccharidosis type II: Lessons learned.
Mol Genet Metab. 2023 Sep-Oct;140(1-2):107557. doi: 10.1016/j.ymgme.2023.107557. Epub 2023 Mar 6.
Mol Genet Metab. 2023.
PMID: 36907694
Newborn Screening for X-Linked Adrenoleukodystrophy: The Initial Illinois Experience.
Burton BK, Hickey R, Hitchins L, Shively V, Ehrhardt J, Ashbaugh L, Peng Y, Basheeruddin K.
Burton BK, et al. Among authors: ehrhardt j.
Int J Neonatal Screen. 2022 Jan 17;8(1):6. doi: 10.3390/ijns8010006.
Int J Neonatal Screen. 2022.
PMID: 35076462
Free PMC article.
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Utilizing Public Health Frameworks and Partnerships to Ensure Equity in DNA-Based Population Screening.
Azriel E, Henley C, Ehrhardt J, Hampel H, Newlin A, Ramos E, Wicklund C, Duquette D.
Azriel E, et al. Among authors: ehrhardt j.
Front Genet. 2022 May 13;13:886755. doi: 10.3389/fgene.2022.886755. eCollection 2022.
Front Genet. 2022.
PMID: 35646064
Free PMC article.
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Selected birth defects data from population-based birth defects surveillance programs in the United States, 2005–2009: Featuring critical congenital heart defects targeted for pulse oximetry screening.
Mai CT, Riehle-Colarusso T, O'Halloran A, Cragan JD, Olney RS, Lin A, Feldkamp M, Botto LD, Rickard R, Anderka M, Ethen M, Stanton C, Ehrhardt J, Canfield M; National Birth Defects Prevention Network.
Mai CT, et al. Among authors: ehrhardt j.
Birth Defects Res A Clin Mol Teratol. 2012 Dec;94(12):970-83. doi: 10.1002/bdra.23098.
Birth Defects Res A Clin Mol Teratol. 2012.
PMID: 24083317
Free PMC article.
No abstract available.
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