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A de novo deletion in a boy with cerebral palsy suggests a refined critical region for the 4q21.22 microdeletion syndrome.
Am J Med Genet A. 2017 May;173(5):1287-1293. doi: 10.1002/ajmg.a.38176. Epub 2017 Apr 3.
Am J Med Genet A. 2017.
PMID: 28371330
No, it is not mutually exclusive! A case report of a girl with two genetic diagnoses: Craniofrontonasal dysplasia and pontocerebellar hypoplasia type 1B.
Ibrahim I, Scriver T, Basalom SA.
Ibrahim I, et al. Among authors: scriver t.
Clin Case Rep. 2023 May 10;11(5):e7332. doi: 10.1002/ccr3.7332. eCollection 2023 May.
Clin Case Rep. 2023.
PMID: 37180334
Free PMC article.
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Erlotinib, gefitinib, and vandetanib inhibit human nucleoside transporters and protect cancer cells from gemcitabine cytotoxicity.
Damaraju VL, Scriver T, Mowles D, Kuzma M, Ryan AJ, Cass CE, Sawyer MB.
Damaraju VL, et al. Among authors: scriver t.
Clin Cancer Res. 2014 Jan 1;20(1):176-86. doi: 10.1158/1078-0432.CCR-13-2293. Epub 2013 Oct 29.
Clin Cancer Res. 2014.
PMID: 24170548
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