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Page 1
Limits of clinical assessment in the accurate diagnosis of Machado-Joseph disease.
Lopes-Cendes I, Silveira I, Maciel P, Gaspar C, Radvany J, Chitayat D, Babul R, Stewart J, Dolliver M, Robitaille Y, Rouleau GA, Sequeiros J. Lopes-Cendes I, et al. Among authors: babul r. Arch Neurol. 1996 Nov;53(11):1168-74. doi: 10.1001/archneur.1996.00550110120020. Arch Neurol. 1996. PMID: 8912491
Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patients.
Silveira I, Lopes-Cendes I, Kish S, Maciel P, Gaspar C, Coutinho P, Botez MI, Teive H, Arruda W, Steiner CE, Pinto-Júnior W, Maciel JA, Jerin S, Sack G, Andermann E, Sudarsky L, Rosenberg R, MacLeod P, Chitayat D, Babul R, Sequeiros J, Rouleau GA. Silveira I, et al. Among authors: babul r. Neurology. 1996 Jan;46(1):214-8. doi: 10.1212/wnl.46.1.214. Neurology. 1996. PMID: 8559378
Linkage analysis of the nail-patella syndrome.
Campeau E, Watkins D, Rouleau GA, Babul R, Buchanan JA, Meschino W, Der Kaloustian VM. Campeau E, et al. Among authors: babul r. Am J Hum Genet. 1995 Jan;56(1):243-7. Am J Hum Genet. 1995. PMID: 7825584 Free PMC article.
Omphalocele in Miller-Dieker syndrome: expanding the phenotype.
Chitayat D, Toi A, Babul R, Blaser S, Moola S, Yarkoni D, Sermer M, Johnson JA, Vasjar J, Teshima I. Chitayat D, et al. Among authors: babul r. Am J Med Genet. 1997 Mar 31;69(3):293-8. doi: 10.1002/(sici)1096-8628(19970331)69:3<293::aid-ajmg15>3.0.co;2-m. Am J Med Genet. 1997. PMID: 9096760
Limb defects in homozygous alpha-thalassemia: report of three cases.
Chitayat D, Silver MM, O'Brien K, Wyatt P, Waye JS, Chiu DH, Babul R, Thomas M. Chitayat D, et al. Among authors: babul r. Am J Med Genet. 1997 Jan 20;68(2):162-7. doi: 10.1002/(sici)1096-8628(19970120)68:2<162::aid-ajmg8>3.0.co;2-r. Am J Med Genet. 1997. PMID: 9028451
11 results