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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2019 | 1 |
2022 | 1 |
2023 | 1 |
2024 | 0 |
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Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individuals.
Genet Med. 2023 Nov;25(11):100950. doi: 10.1016/j.gim.2023.100950. Epub 2023 Aug 5.
Genet Med. 2023.
PMID: 37551667
Free article.
Ultrathin wide band gap kesterites.
Platzer Björkman C, Larsen JK, Saini N, Babucci M, Martin N.
Platzer Björkman C, et al.
Faraday Discuss. 2022 Oct 28;239(0):38-50. doi: 10.1039/d2fd00052k.
Faraday Discuss. 2022.
PMID: 35916023
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De Novo Variants in MAPK8IP3 Cause Intellectual Disability with Variable Brain Anomalies.
Platzer K, Sticht H, Edwards SL, Allen W, Angione KM, Bonati MT, Brasington C, Cho MT, Demmer LA, Falik-Zaccai T, Gamble CN, Hellenbroich Y, Iascone M, Kok F, Mahida S, Mandel H, Marquardt T, McWalter K, Panis B, Pepler A, Pinz H, Ramos L, Shinde DN, Smith-Hicks C, Stegmann APA, Stöbe P, Stumpel CTRM, Wilson C, Lemke JR, Di Donato N, Miller KG, Jamra R.
Platzer K, et al.
Am J Hum Genet. 2019 Feb 7;104(2):203-212. doi: 10.1016/j.ajhg.2018.12.008. Epub 2019 Jan 3.
Am J Hum Genet. 2019.
PMID: 30612693
Free PMC article.
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