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Decision-making process for conditions nominated to the recommended uniform screening panel: statement of the US Department of Health and Human Services Secretary's Advisory Committee on Heritable Disorders in Newborns and Children.
Kemper AR, Green NS, Calonge N, Lam WK, Comeau AM, Goldenberg AJ, Ojodu J, Prosser LA, Tanksley S, Bocchini JA Jr. Kemper AR, et al. Among authors: comeau am. Genet Med. 2014 Feb;16(2):183-7. doi: 10.1038/gim.2013.98. Epub 2013 Aug 1. Genet Med. 2014. PMID: 23907646 Free article.
Case Definitions for Conditions Identified by Newborn Screening Public Health Surveillance.
Sontag MK, Sarkar D, Comeau AM, Hassell K, Botto LD, Parad R, Rose SR, Wintergerst KA, Smith-Whitley K, Singh S, Yusuf C, Ojodu J, Copeland S, Hinton CF. Sontag MK, et al. Among authors: comeau am. Int J Neonatal Screen. 2018;4(2):16. doi: 10.3390/ijns4020016. Epub 2018 May 9. Int J Neonatal Screen. 2018. PMID: 29862374 Free PMC article.
An evidence development process for newborn screening.
Perrin JM, Knapp AA, Browning MF, Comeau AM, Green NS, Lipstein EA, Metterville DR, Prosser L, Queally D, Kemper AR. Perrin JM, et al. Among authors: comeau am. Genet Med. 2010 Mar;12(3):131-4. doi: 10.1097/GIM.0b013e3181d28eb1. Genet Med. 2010. PMID: 20154629 Free article. Review. No abstract available.
129 results