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

Year Number of Results
1998 1
2003 1
2004 1
2005 1
2006 1
2008 1
2009 1
2010 1
2011 1
2012 1
2013 2
2014 5
2015 4
2016 6
2017 3
2018 5
2019 5
2020 6
2021 4
2022 1
2023 4
2024 0

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Page 1
Position statement from the International Society for Prenatal Diagnosis on the use of non-invasive prenatal testing for the detection of fetal chromosomal conditions in singleton pregnancies.
Hui L, Ellis K, Mayen D, Pertile MD, Reimers R, Sun L, Vermeesch J, Vora NL, Chitty LS. Hui L, et al. Among authors: pertile md. Prenat Diagn. 2023 Jun;43(7):814-828. doi: 10.1002/pd.6357. Epub 2023 May 16. Prenat Diagn. 2023. PMID: 37076973 No abstract available.
Questionable pathogenicity of FOXG1 duplication.
Amor DJ, Burgess T, Tan TY, Pertile MD. Amor DJ, et al. Among authors: pertile md. Eur J Hum Genet. 2012 Jun;20(6):595-6; author reply 596-7. doi: 10.1038/ejhg.2011.267. Epub 2012 Jan 18. Eur J Hum Genet. 2012. PMID: 22258524 Free PMC article. No abstract available.
Exceptional complex chromosomal rearrangements in three generations.
Kartapradja H, Marzuki NS, Pertile MD, Francis D, Suciati LP, Anggaratri HW, Ambarwati DD, Idris FP, Lesmana H, Trimarsanto H, Paramayuda C, Harahap AR. Kartapradja H, et al. Among authors: pertile md. Case Rep Genet. 2015;2015:321014. doi: 10.1155/2015/321014. Epub 2015 Feb 3. Case Rep Genet. 2015. PMID: 25722897 Free PMC article.
Haplotyping the human leukocyte antigen system from single chromosomes.
Murphy NM, Burton M, Powell DR, Rossello FJ, Cooper D, Chopra A, Hsieh MJ, Sayer DC, Gordon L, Pertile MD, Tait BD, Irving HR, Pouton CW. Murphy NM, et al. Among authors: pertile md. Sci Rep. 2016 Jul 27;6:30381. doi: 10.1038/srep30381. Sci Rep. 2016. PMID: 27461731 Free PMC article.
48 results