Published in J Clin Endocrinol Metab on August 01, 1983
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The -158 site 5' to the G gamma gene and G gamma expression. Blood (1985) 1.34
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The absence of correlation between allozyme and rrn RFLP analysis indicates a high gene flow rate within human clinical Pseudomonas aeruginosa isolates. FEMS Microbiol Lett (1993) 1.32
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Molecular analysis provides evidence for the endogenous origin of bacteremia and meningitis due to Enterobacter cloacae in an infant. Clin Infect Dis (1992) 1.24
A novel sickle cell mutation of yet another origin in Africa: the Cameroon type. Hum Genet (1992) 1.23
Characterization of highly virulent Escherichia coli strains by ribosomal DNA restriction fragment length polymorphism. FEMS Microbiol Lett (1991) 1.23
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Rapid genotyping shows the absence of cross-contamination in Enterobacter cloacae nosocomial infections. J Hosp Infect (1992) 1.21
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Usefulness of omp1 restriction mapping for avian Chlamydia psittaci isolate differentiation. Res Microbiol (1995) 1.19
Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome. Am J Hum Genet (2001) 1.19
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Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers. Am J Hum Genet (1994) 1.15
Comparison of octreotide acetate LAR and lanreotide SR in patients with acromegaly. Clin Endocrinol (Oxf) (2000) 1.15
Description and partial characterization of a new Chlamydia-like microorganism. FEMS Microbiol Lett (1993) 1.14
Beta-chain contact sites in the haemoglobin S polymer. Nature (1980) 1.13
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Structural and functional abnormalities at 11p15 are associated with the malignant phenotype in sporadic adrenocortical tumors: study on a series of 82 tumors. J Clin Endocrinol Metab (1997) 1.12
Ribotyping provides efficient differentiation of nosocomial Serratia marcescens isolates in a pediatric hospital. J Clin Microbiol (1992) 1.12
Reversible gonadotropin deficiency in male Cushing's disease. J Clin Endocrinol Metab (1977) 1.11
Covalent structures of beta and gamma autolytic derivatives of human alpha-thrombin. J Biol Chem (1984) 1.11
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Mother-to-child transmitted WT1 splice-site mutation is responsible for distinct glomerular diseases. J Am Soc Nephrol (1999) 1.10
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Cholestasis and biliary dilatation associated with chronic ketamine abuse: a case series. Singapore Med J (2011) 1.09
Assessment of heavy metals (Cd, Cr and Pb) in water, sediment and seaweed (Ulva lactuca) in the Pulicat Lake, South East India. Chemosphere (2008) 1.09
Reverse cascade screening of newborns for hereditary haemochromatosis: a model for other late onset diseases? J Med Genet (2005) 1.08
Allele and genotype frequency of CYP2C19 in a Tamilian population. Br J Clin Pharmacol (2003) 1.08
DNA sequence variation in a negative control region 5' to the beta-globin gene correlates with the phenotypic expression of the beta s mutation. Blood (1992) 1.08
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Spectrum of beta thalassemia mutations and their linkage to beta-globin gene haplotypes in the Indo-Mauritians. Am J Hematol (2000) 1.08
Evidence of an endogenous digitalis-like factor in the plasma of patients with acromegaly. N Engl J Med (1987) 1.08