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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 1
2004 2
2005 2
2007 1
2010 1
2011 1
2012 2
2013 1
2016 1
2017 1
2019 1
2020 1
2021 2
2023 2
2024 0

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17 results

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Page 1
Newborn Screening: Current Status in Alberta, Canada.
De Souza A, Wolan V, Battochio A, Christian S, Hume S, Johner G, Lilley M, Ridsdale R, Schnabl K, Tran C, Yuen-Jung J, Sosova I. De Souza A, et al. Among authors: lilley m. Int J Neonatal Screen. 2019 Oct 1;5(4):37. doi: 10.3390/ijns5040037. eCollection 2019 Dec. Int J Neonatal Screen. 2019. PMID: 33072996 Free PMC article. Review.
Interconceptional counseling after perinatal and infant loss.
Wallerstedt C, Lilley M, Baldwin K. Wallerstedt C, et al. Among authors: lilley m. J Obstet Gynecol Neonatal Nurs. 2003 Jul-Aug;32(4):533-42. doi: 10.1177/0884217503255264. J Obstet Gynecol Neonatal Nurs. 2003. PMID: 12903704 Review.
Secondary Reporting of G6PD Deficiency on Newborn Screening.
Hoang SC, Blumenschein P, Lilley M, Olshaski L, Bruce A, Wright NAM, Ridsdale R, Christian S. Hoang SC, et al. Among authors: lilley m. Int J Neonatal Screen. 2023 Mar 27;9(2):18. doi: 10.3390/ijns9020018. Int J Neonatal Screen. 2023. PMID: 37092512 Free PMC article.
Alberta Spinal Muscular Atrophy Newborn Screening-Results from Year 1 Pilot Project.
Niri F, Nicholls J, Baptista Wyatt K, Walker C, Price T, Kelln R, Hume S, Parboosingh J, Lilley M, Kolski H, Ridsdale R, Muranyi A, Mah JK, Bulman DE. Niri F, et al. Among authors: lilley m. Int J Neonatal Screen. 2023 Jul 27;9(3):42. doi: 10.3390/ijns9030042. Int J Neonatal Screen. 2023. PMID: 37606479 Free PMC article.
Sickle cell trait newborn screen results: disclosure and management.
Lilley M, Hoang S, Blumenschein P, Peturson AM, Sosova I, Macneil L, Ridsdale R, Christian S. Lilley M, et al. J Community Genet. 2021 Jan;12(1):137-142. doi: 10.1007/s12687-020-00489-x. Epub 2020 Oct 26. J Community Genet. 2021. PMID: 33106985 Free PMC article.
Further Defining the Role of the Laboratory Genetic Counselor.
Waltman L, Runke C, Balcom J, Riley JD, Lilley M, Christian S, Zetzsche L, Goodenberger ML. Waltman L, et al. Among authors: lilley m. J Genet Couns. 2016 Aug;25(4):786-98. doi: 10.1007/s10897-015-9927-4. Epub 2016 Feb 20. J Genet Couns. 2016. PMID: 26895873
Defining the role of laboratory genetic counselor.
Christian S, Lilley M, Hume S, Scott P, Somerville M. Christian S, et al. Among authors: lilley m. J Genet Couns. 2012 Aug;21(4):605-11. doi: 10.1007/s10897-011-9419-0. Epub 2011 Nov 11. J Genet Couns. 2012. PMID: 22075756
Microduplication and triplication of 22q11.2: a highly variable syndrome.
Yobb TM, Somerville MJ, Willatt L, Firth HV, Harrison K, MacKenzie J, Gallo N, Morrow BE, Shaffer LG, Babcock M, Chernos J, Bernier F, Sprysak K, Christiansen J, Haase S, Elyas B, Lilley M, Bamforth S, McDermid HE. Yobb TM, et al. Among authors: lilley m. Am J Hum Genet. 2005 May;76(5):865-76. doi: 10.1086/429841. Epub 2005 Mar 30. Am J Hum Genet. 2005. PMID: 15800846 Free PMC article.
17 results