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

Year Number of Results
1982 1
1983 1
1987 1
1988 1
1994 1
1998 1
1999 3
2001 2
2002 2
2004 2
2007 1
2008 4
2009 1
2011 5
2012 1
2013 1
2014 4
2015 1
2016 3
2017 4
2018 8
2019 6
2020 22
2021 23
2022 8
2023 12
2024 2

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104 results

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Page 1
Consensus recommendations on Epilepsy in Phelan-McDermid syndrome.
de Coo IFM, Jesse S, Le TL, Sala C; European Phelan-McDermid syndrome consortium. de Coo IFM, et al. Among authors: le tl. Eur J Med Genet. 2023 Jun;66(6):104746. doi: 10.1016/j.ejmg.2023.104746. Epub 2023 Mar 24. Eur J Med Genet. 2023. PMID: 36967043 Free article. Review.
Microfluidic CARS cytometry.
Wang HW, Bao N, Le TL, Lu C, Cheng JX. Wang HW, et al. Among authors: le tl. Opt Express. 2008 Apr 14;16(8):5782-9. doi: 10.1364/oe.16.005782. Opt Express. 2008. PMID: 18542688 Free PMC article.
Bi-allelic loss-of-function variants in WBP4, encoding a spliceosome protein, result in a variable neurodevelopmental syndrome.
Engal E, Oja KT, Maroofian R, Geminder O, Le TL, Marzin P, Guimier A, Mor E, Zvi N, Elefant N, Zaki MS, Gleeson JG, Muru K, Pajusalu S, Wojcik MH, Pachat D, Elmaksoud MA, Chan Jeong W, Lee H, Bauer P, Zifarelli G, Houlden H, Daana M, Elpeleg O, Amiel J, Lyonnet S, Gordon CT, Harel T, Õunap K, Salton M, Mor-Shaked H. Engal E, et al. Among authors: le tl. Am J Hum Genet. 2023 Dec 7;110(12):2112-2119. doi: 10.1016/j.ajhg.2023.10.013. Epub 2023 Nov 13. Am J Hum Genet. 2023. PMID: 37963460
First report from the Asian Rotavirus Surveillance Network.
Bresee J, Fang ZY, Wang B, Nelson EA, Tam J, Soenarto Y, Wilopo SA, Kilgore P, Kim JS, Kang JO, Lan WS, Gaik CL, Moe K, Chen KT, Jiraphongsa C, Ponguswanna Y, Nguyen VM, Phan VT, Le TL, Hummelman E, Gentsch JR, Glass R; Asian Rotavirus Surveillance Network. Bresee J, et al. Among authors: le tl. Emerg Infect Dis. 2004 Jun;10(6):988-95. doi: 10.3201/eid1006.030519. Emerg Infect Dis. 2004. PMID: 15207047 Free PMC article. Review.
Mechanisms of mRNA processing defects in inherited THOC6 intellectual disability syndrome.
Werren E, LaForce G, Srivastava A, Perillo D, Johnson K, Berger B, Regan S, Pfennig C, Baris S, de Munnik S, Pfundt R, Hebbar M, Jimenez Heredia R, Karakoc-Aydiner E, Ozen A, Dmytrus J, Krolo A, Corning K, Prijoles E, Louie R, Lebel R, Le TL, Amiel J, Gordon C, Boztug K, Girisha K, Shukla A, Bielas S, Schaffer A. Werren E, et al. Among authors: le tl. Res Sq [Preprint]. 2023 Sep 6:rs.3.rs-2126145. doi: 10.21203/rs.3.rs-2126145/v1. Res Sq. 2023. PMID: 37720017 Free PMC article. Updated. Preprint.
104 results