Published in Trends Biochem Sci on May 01, 1988
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Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studies. Am J Hum Genet (1993) 1.16
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Dinucleotide repeat polymorphism at D16S287. Nucleic Acids Res (1991) 1.11
Predictive diagnosis of myotonic dystrophy with flanking microsatellite markers. J Med Genet (1991) 1.10
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Characterization of a deletion at Xq27-q28 associated with unbalanced inactivation of the nonmutant X chromosome. Am J Hum Genet (1992) 1.02
A 5' flanking region of the metallothionein, MT2A, gene identifies two moderately frequent RFLPs. Nucleic Acids Res (1987) 1.00
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Acinetobacter baumannii: emergence of four strains with novel bla(OXA-51-like) genes in patients with diabetes mellitus. J Chemother (2009) 0.99
Schistosomiasis. ...contrary to popular belief. BMJ (1993) 0.99
Autosomal dominant congenital non-progressive ataxia overlaps with the SCA15 locus. Neurology (2004) 0.99
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Linkage disequilibrium mapping places the gene causing familial Mediterranean fever close to D16S246. Am J Hum Genet (1996) 0.97
Vaginal pH and microflora related to yeast infections and treatment. Br J Vener Dis (1980) 0.96
Functional and molecular evidence for beta 1-, beta 2- and beta 3- adrenoceptors in human colon. Br J Pharmacol (1997) 0.96
Experience with direct molecular diagnosis of fragile X. J Med Genet (1992) 0.95
Complete androgen insensitivity syndrome characterized by increased concentration of a normal androgen receptor in genital skin fibroblasts. J Clin Endocrinol Metab (1986) 0.95
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