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Page 1
22q11.2 deletion syndrome.
McDonald-McGinn DM, Sullivan KE, Marino B, Philip N, Swillen A, Vorstman JA, Zackai EH, Emanuel BS, Vermeesch JR, Morrow BE, Scambler PJ, Bassett AS. McDonald-McGinn DM, et al. Nat Rev Dis Primers. 2015 Nov 19;1:15071. doi: 10.1038/nrdp.2015.71. Nat Rev Dis Primers. 2015. PMID: 27189754 Free PMC article. Review.
Age-Related Parkinsonian Signs in Microdeletion 22q11.2.
Boot E, Mentzel TQ, Palmer LD, van Harten PN, Marras C, Lang AE, Bassett AS. Boot E, et al. Mov Disord. 2020 Jul;35(7):1239-1245. doi: 10.1002/mds.28080. Epub 2020 May 9. Mov Disord. 2020. PMID: 32386091 Free PMC article.
Reproductive Outcomes in Adults with 22q11.2 Deletion Syndrome.
Palmer LD, McManus Z, Heung T, McAlpine G, Blagojevic C, Corral M, Bassett AS. Palmer LD, et al. Genes (Basel). 2022 Nov 16;13(11):2126. doi: 10.3390/genes13112126. Genes (Basel). 2022. PMID: 36421801 Free PMC article.
Genome-wide tandem repeat expansions contribute to schizophrenia risk.
Mojarad BA, Engchuan W, Trost B, Backstrom I, Yin Y, Thiruvahindrapuram B, Pallotto L, Mitina A, Khan M, Pellecchia G, Haque B, Guo K, Heung T, Costain G, Scherer SW, Marshall CR, Pearson CE, Bassett AS, Yuen RKC. Mojarad BA, et al. Mol Psychiatry. 2022 Sep;27(9):3692-3698. doi: 10.1038/s41380-022-01575-x. Epub 2022 May 12. Mol Psychiatry. 2022. PMID: 35546631 Free PMC article.
Elucidating the diagnostic odyssey of 22q11.2 deletion syndrome.
Palmer LD, Butcher NJ, Boot E, Hodgkinson KA, Heung T, Chow EWC, Guna A, Crowley TB, Zackai E, McDonald-McGinn DM, Bassett AS. Palmer LD, et al. Am J Med Genet A. 2018 Apr;176(4):936-944. doi: 10.1002/ajmg.a.38645. Am J Med Genet A. 2018. PMID: 29575622 Free PMC article.
16 results