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An algorithm to identify patients aged 0-3 with rare genetic disorders.
Webb BD, Lau LY, Tsevdos D, Shewcraft RA, Corrigan D, Shi L, Lee S, Tyler J, Li S, Wang Z, Stolovitzky G, Edelmann L, Chen R, Schadt EE, Li L. Webb BD, et al. Among authors: lau ly. Orphanet J Rare Dis. 2024 May 2;19(1):183. doi: 10.1186/s13023-024-03188-9. Orphanet J Rare Dis. 2024. PMID: 38698482 Free PMC article.
A recurrent SHANK3 frameshift variant in Autism Spectrum Disorder.
Loureiro LO, Howe JL, Reuter MS, Iaboni A, Calli K, Roshandel D, Pritišanac I, Moses A, Forman-Kay JD, Trost B, Zarrei M, Rennie O, Lau LYS, Marshall CR, Srivastava S, Godlewski B, Buttermore ED, Sahin M, Hartley D, Frazier T, Vorstman J, Georgiades S, Lewis SME, Szatmari P, Bradley CAL, Tabet AC, Willems M, Lumbroso S, Piton A, Lespinasse J, Delorme R, Bourgeron T, Anagnostou E, Scherer SW. Loureiro LO, et al. Among authors: lau lys. NPJ Genom Med. 2021 Nov 4;6(1):91. doi: 10.1038/s41525-021-00254-0. NPJ Genom Med. 2021. PMID: 34737294 Free PMC article.
Virtual reality simulation training in Otolaryngology.
Arora A, Lau LY, Awad Z, Darzi A, Singh A, Tolley N. Arora A, et al. Among authors: lau ly. Int J Surg. 2014;12(2):87-94. doi: 10.1016/j.ijsu.2013.11.007. Epub 2013 Dec 5. Int J Surg. 2014. PMID: 24316019 Free article. Review.
12 results