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Results of a genome-wide linkage scan for stuttering.
Shugart YY, Mundorff J, Kilshaw J, Doheny K, Doan B, Wanyee J, Green ED, Drayna D. Shugart YY, et al. Among authors: drayna d. Am J Med Genet A. 2004 Jan 15;124A(2):133-5. doi: 10.1002/ajmg.a.20347. Am J Med Genet A. 2004. PMID: 14699610
The sex ratio in familial persistent stuttering.
Drayna D, Kilshaw J, Kelly J. Drayna D, et al. Am J Hum Genet. 1999 Nov;65(5):1473-5. doi: 10.1086/302625. Am J Hum Genet. 1999. PMID: 10521318 Free PMC article. No abstract available.
Genomewide significant linkage to stuttering on chromosome 12.
Riaz N, Steinberg S, Ahmad J, Pluzhnikov A, Riazuddin S, Cox NJ, Drayna D. Riaz N, et al. Among authors: drayna d. Am J Hum Genet. 2005 Apr;76(4):647-51. doi: 10.1086/429226. Epub 2005 Feb 15. Am J Hum Genet. 2005. PMID: 15714404 Free PMC article.
Mucolipidosis types II and III and non-syndromic stuttering are associated with different variants in the same genes.
Raza MH, Domingues CE, Webster R, Sainz E, Paris E, Rahn R, Gutierrez J, Chow HM, Mundorff J, Kang CS, Riaz N, Basra MA, Khan S, Riazuddin S, Moretti-Ferreira D, Braun A, Drayna D. Raza MH, et al. Among authors: drayna d. Eur J Hum Genet. 2016 Apr;24(4):529-34. doi: 10.1038/ejhg.2015.154. Epub 2015 Jul 1. Eur J Hum Genet. 2016. PMID: 26130485 Free PMC article.
111 results