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Page 1
Genetic studies of autistic disorder and chromosome 7.
Ashley-Koch A, Wolpert CM, Menold MM, Zaeem L, Basu S, Donnelly SL, Ravan SA, Powell CM, Qumsiyeh MB, Aylsworth AS, Vance JM, Gilbert JR, Wright HH, Abramson RK, DeLong GR, Cuccaro ML, Pericak-Vance MA. Ashley-Koch A, et al. Genomics. 1999 Nov 1;61(3):227-36. doi: 10.1006/geno.1999.5968. Genomics. 1999. PMID: 10552924
A second leaky splice-site mutation in the spastin gene.
Svenson IK, Ashley-Koch AE, Pericak-Vance MA, Marchuk DA. Svenson IK, et al. Am J Hum Genet. 2001 Dec;69(6):1407-9. doi: 10.1086/324593. Am J Hum Genet. 2001. PMID: 11704932 Free PMC article. No abstract available.
Genomic screen and follow-up analysis for autistic disorder.
Shao Y, Wolpert CM, Raiford KL, Menold MM, Donnelly SL, Ravan SA, Bass MP, McClain C, von Wendt L, Vance JM, Abramson RH, Wright HH, Ashley-Koch A, Gilbert JR, DeLong RG, Cuccaro ML, Pericak-Vance MA. Shao Y, et al. Am J Med Genet. 2002 Jan 8;114(1):99-105. doi: 10.1002/ajmg.10153. Am J Med Genet. 2002. PMID: 11840513
No association between the WNT2 gene and autistic disorder.
McCoy PA, Shao Y, Wolpert CM, Donnelly SL, Ashley-Koch A, Abel HL, Ravan SA, Abramson RK, Wright HH, DeLong GR, Cuccaro ML, Gilbert JR, Pericak-Vance MA. McCoy PA, et al. Am J Med Genet. 2002 Jan 8;114(1):106-9. doi: 10.1002/ajmg.10182. Am J Med Genet. 2002. PMID: 11840514
A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10).
Reid E, Kloos M, Ashley-Koch A, Hughes L, Bevan S, Svenson IK, Graham FL, Gaskell PC, Dearlove A, Pericak-Vance MA, Rubinsztein DC, Marchuk DA. Reid E, et al. Am J Hum Genet. 2002 Nov;71(5):1189-94. doi: 10.1086/344210. Epub 2002 Sep 24. Am J Hum Genet. 2002. PMID: 12355402 Free PMC article.
273 results