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Page 1
Reduced penetrance of the Huntington's disease mutation.
McNeil SM, Novelletto A, Srinidhi J, Barnes G, Kornbluth I, Altherr MR, Wasmuth JJ, Gusella JF, MacDonald ME, Myers RH. McNeil SM, et al. Hum Mol Genet. 1997 May;6(5):775-9. doi: 10.1093/hmg/6.5.775. Hum Mol Genet. 1997. PMID: 9158152
IT15 gene expression in fetal human brain.
Dure LS 4th, Landwehrmeyer GB, Golden J, McNeil SM, Ge P, Aizawa H, Huang Q, Ambrose CM, Duyao MP, Bird ED, et al. Dure LS 4th, et al. Among authors: mcneil sm. Brain Res. 1994 Oct 3;659(1-2):33-41. doi: 10.1016/0006-8993(94)90860-5. Brain Res. 1994. PMID: 7820679
Inactivation of the mouse Huntington's disease gene homolog Hdh.
Duyao MP, Auerbach AB, Ryan A, Persichetti F, Barnes GT, McNeil SM, Ge P, Vonsattel JP, Gusella JF, Joyner AL, et al. Duyao MP, et al. Among authors: mcneil sm. Science. 1995 Jul 21;269(5222):407-10. doi: 10.1126/science.7618107. Science. 1995. PMID: 7618107
Factors associated with HD CAG repeat instability in Huntington disease.
Wheeler VC, Persichetti F, McNeil SM, Mysore JS, Mysore SS, MacDonald ME, Myers RH, Gusella JF, Wexler NS; US-Venezuela Collaborative Research Group. Wheeler VC, et al. Among authors: mcneil sm. J Med Genet. 2007 Nov;44(11):695-701. doi: 10.1136/jmg.2007.050930. Epub 2007 Jul 27. J Med Genet. 2007. PMID: 17660463 Free PMC article.
12 results