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Results: 1-13 |
Results: 13
Real-time polymerase chain reaction with fluorescent hybridization probes for the detection of prevalent mutations causing common thrombophilic and iron overload phenotypes
Authors: Parks, SB Popovich, BW Press, RD
Citation: Sb. Parks et al., Real-time polymerase chain reaction with fluorescent hybridization probes for the detection of prevalent mutations causing common thrombophilic and iron overload phenotypes, AM J CLIN P, 115(3), 2001, pp. 439-447
Linked linear amplification: A new method for the amplification of DNA
Authors: Reyes, AA Ugozzoli, LA Lowery, JD Breneman, JW Hixson, CS Press, RD Wallace, RB
Citation: Aa. Reyes et al., Linked linear amplification: A new method for the amplification of DNA, CLIN CHEM, 47(1), 2001, pp. 31-40
Iron beware: A common HFE gene polymorphism may prevent the accurate molecular diagnosis of homozygous hemochromatosis in low-risk, but not high-riskgroups
Authors: Press, RD
Citation: Rd. Press, Iron beware: A common HFE gene polymorphism may prevent the accurate molecular diagnosis of homozygous hemochromatosis in low-risk, but not high-riskgroups, HEPATOLOGY, 31(2), 2000, pp. 540-542
Detection of prevalent genetic alterations predisposing to hemochromatosisand other common human diseases
Authors: Press, RD
Citation: Rd. Press, Detection of prevalent genetic alterations predisposing to hemochromatosisand other common human diseases, CLIN CHEM, 46(10), 2000, pp. 1526-1528
Hemochromatosis: A "simple" genetic trait
Authors: Press, RD
Citation: Rd. Press, Hemochromatosis: A "simple" genetic trait, HOSP PRACT, 34(8), 1999, pp. 55
Overestimation of HFE C282Y homozygous hemochromatosis prevalence as the result of a common primer-binding site polymorphism
Authors: Press, RD
Citation: Rd. Press, Overestimation of HFE C282Y homozygous hemochromatosis prevalence as the result of a common primer-binding site polymorphism, MOL DIAGN, 4(4), 1999, pp. 391-392
GeneClinics Medical Genetics Knowledge Base
Authors: Press, RD
Citation: Rd. Press, GeneClinics Medical Genetics Knowledge Base, MOL DIAGN, 4(3), 1999, pp. 256-256
Analyte-specific reagents
Authors: Press, RD
Citation: Rd. Press, Analyte-specific reagents, MOL DIAGN, 4(1), 1999, pp. 71-71
Directories of molecular diagnostic tests and testing laboratories
Authors: Press, RD
Citation: Rd. Press, Directories of molecular diagnostic tests and testing laboratories, MOL DIAGN, 4(1), 1999, pp. 71-72
Exclusivity in testing for patented disease genes
Authors: Press, RD
Citation: Rd. Press, Exclusivity in testing for patented disease genes, MOL DIAGN, 4(1), 1999, pp. 72-73
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results
Authors: Gomez, PS Parks, S Ries, R Tran, TC Gomez, PF Press, RD
Citation: Ps. Gomez et al., Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results, NAT GENET, 23(3), 1999, pp. 272-272
Role of a common mutation in the homocysteine regulatory enzyme methylenetetrahydrofolate reductase in ischemic stroke
Authors: Press, RD Beamer, N Evans, A DeLoughery, TG Coull, BM
Citation: Rd. Press et al., Role of a common mutation in the homocysteine regulatory enzyme methylenetetrahydrofolate reductase in ischemic stroke, DIAGN MOL P, 8(1), 1999, pp. 54-58
Hereditary hemochromatosis - Impact of molecular and iron-based testing onthe diagnosis, treatment, and prevention of a common, chronic disease
Authors: Press, RD
Citation: Rd. Press, Hereditary hemochromatosis - Impact of molecular and iron-based testing onthe diagnosis, treatment, and prevention of a common, chronic disease, ARCH PATH L, 123(11), 1999, pp. 1053-1059
Risultati: 1-13 |