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Inherited deletion at Duchenne dystrophy locus in normal male.
Bartlett RJ, Walker AP, Laing NG, Koh J, Secore SL, Speer MC, Pericak-Vance M, Hung WY, Yamaoka LH, Siddique T, et al. Bartlett RJ, et al. Lancet. 1989 Mar 4;1(8636):496-7. doi: 10.1016/s0140-6736(89)91394-9. Lancet. 1989. PMID: 2563864 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
A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families: evidence for a major susceptibility locus on chromosome 2p.
Pillai SG, Chiano MN, White NJ, Speer M, Barnes KC, Carlsen K, Gerritsen J, Helms P, Lenney W, Silverman M, Sly P, Sundy J, Tsanakas J, von Berg A, Whyte M, Varsani S, Skelding P, Hauser M, Vance J, Pericak-Vance M, Burns DK, Middleton LT, Brewster SR, Anderson WH, Riley JH. Pillai SG, et al. Eur J Hum Genet. 2006 Mar;14(3):307-16. doi: 10.1038/sj.ejhg.5201532. Eur J Hum Genet. 2006. PMID: 16391567
Identification of TMEM230 mutations in familial Parkinson's disease.
Deng HX, Shi Y, Yang Y, Ahmeti KB, Miller N, Huang C, Cheng L, Zhai H, Deng S, Nuytemans K, Corbett NJ, Kim MJ, Deng H, Tang B, Yang Z, Xu Y, Chan P, Huang B, Gao XP, Song Z, Liu Z, Fecto F, Siddique N, Foroud T, Jankovic J, Ghetti B, Nicholson DA, Krainc D, Melen O, Vance JM, Pericak-Vance MA, Ma YC, Rajput AH, Siddique T. Deng HX, et al. Nat Genet. 2016 Jul;48(7):733-9. doi: 10.1038/ng.3589. Epub 2016 Jun 6. Nat Genet. 2016. PMID: 27270108 Free PMC article.
832 results