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Page 1
Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion.
Saitta SC, Harris SE, Gaeth AP, Driscoll DA, McDonald-McGinn DM, Maisenbacher MK, Yersak JM, Chakraborty PK, Hacker AM, Zackai EH, Ashley T, Emanuel BS. Saitta SC, et al. Among authors: harris se. Hum Mol Genet. 2004 Feb 15;13(4):417-28. doi: 10.1093/hmg/ddh041. Epub 2003 Dec 17. Hum Mol Genet. 2004. PMID: 14681306 Free PMC article.
Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome.
Bearden CE, Jawad AF, Lynch DR, Monterossso JR, Sokol S, McDonald-McGinn DM, Saitta SC, Harris SE, Moss E, Wang PP, Zackai E, Emanuel BS, Simon TJ. Bearden CE, et al. Among authors: harris se. Child Neuropsychol. 2005 Feb;11(1):109-17. doi: 10.1080/09297040590911239. Child Neuropsychol. 2005. PMID: 15846854 Free PMC article.
Fine mapping of the Darier's disease locus on chromosome 12q.
Richard G, Wright AR, Harris S, Doyle SZ, Korge B, Mazzanti C, Tanaka T, Harth W, McBride OW, Compton JG, Bale SJ, DiGiovanna JJ. Richard G, et al. J Invest Dermatol. 1994 Nov;103(5):665-8. doi: 10.1111/1523-1747.ep12398429. J Invest Dermatol. 1994. PMID: 7963653 Free article.
Familial deletion of chromosome 18 (p11.2).
Velagaleti GV, Harris S, Carpenter NJ, Coldwell J, Say B. Velagaleti GV, et al. Ann Genet. 1996;39(4):201-4. Ann Genet. 1996. PMID: 9037347
Visualizing liquid-liquid phase transitions.
Sahoo BR, Deng X, Wong EL, Clark N, Yang H, Subramanian V, Guzman BB, Harris SE, Dehury B, Miyashita E, Hoff JD, Kocaman V, Saito H, Dominguez D, Plavec J, Bardwell JCA. Sahoo BR, et al. Among authors: harris se. bioRxiv [Preprint]. 2024 Oct 28:2023.10.09.561572. doi: 10.1101/2023.10.09.561572. bioRxiv. 2024. PMID: 39554013 Free PMC article. Preprint.
620 results