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Results: 1-11 |
Results: 11
Simultaneous allele-specific amplification: A strategy using modified primer-template mismatches for SNP detection - Application to prothrombin 20210A (factor II) and factor V Leiden (1691A) gene mutations
Authors: Delrio-Lafreniere, SA McGlennen, RC
Citation: Sa. Delrio-lafreniere et Rc. Mcglennen, Simultaneous allele-specific amplification: A strategy using modified primer-template mismatches for SNP detection - Application to prothrombin 20210A (factor II) and factor V Leiden (1691A) gene mutations, MOL DIAGN, 6(3), 2001, pp. 201-209
Miniaturization technologies for molecular diagnostics
Authors: McGlennen, RC
Citation: Rc. Mcglennen, Miniaturization technologies for molecular diagnostics, CLIN CHEM, 47(3), 2001, pp. 393-402
Evaluation of an automated technique for assessment of marrow engraftment after allogeneic bone marrow transplantation using a commercially availablekit
Authors: Nuckols, JD Rasheed, BKA McGlennen, RC Bigner, SH Stenzel, TT
Citation: Jd. Nuckols et al., Evaluation of an automated technique for assessment of marrow engraftment after allogeneic bone marrow transplantation using a commercially availablekit, AM J CLIN P, 113(1), 2000, pp. 135-140
Human papillomavirus oncogenesis
Authors: McGlennen, RC
Citation: Rc. Mcglennen, Human papillomavirus oncogenesis, CLIN LAB M, 20(2), 2000, pp. 383
Non-leukemic autologous reconstitution after allogeneic bone marrow transplantation for Ph-positive chronic myelogenous leukemia: extended remission preceding eventual relapse
Authors: Brunstein, CG Hirsch, BA Miller, JS McGlennen, RC Verfaillie, CM McGlave, PB Weisdorf, DJ
Citation: Cg. Brunstein et al., Non-leukemic autologous reconstitution after allogeneic bone marrow transplantation for Ph-positive chronic myelogenous leukemia: extended remission preceding eventual relapse, BONE MAR TR, 26(11), 2000, pp. 1173-1177
Hereditary spastic paraplegia and hereditary ataxia - Part 2: A family demonstrating various phenotypic manifestations with the SCA3 genotype
Authors: Landau, WM Schmidt, RE McGlennen, RC Reich, SG
Citation: Wm. Landau et al., Hereditary spastic paraplegia and hereditary ataxia - Part 2: A family demonstrating various phenotypic manifestations with the SCA3 genotype, ARCH NEUROL, 57(5), 2000, pp. 733-739
Methods to detect clonal gene rearrangements in lymphomas and leukemias
Authors: Mitha, N McGlennen, RC
Citation: N. Mitha et Rc. Mcglennen, Methods to detect clonal gene rearrangements in lymphomas and leukemias, METH MOL M, 49, 2000, pp. 189-209
Monitoring of bone marrow transplant engraftment
Authors: Woronzoff-Dashkoff, KP McGlennen, RC
Citation: Kp. Woronzoff-dashkoff et Rc. Mcglennen, Monitoring of bone marrow transplant engraftment, METH MOL M, 49, 2000, pp. 211-225
Are benign cellular changes on a Papanicolaou smear really benign? A prospective cohort study
Authors: Margolis, KL Carson, LF Setness, PA Stanley, MW Henry-Stanley, MJ Beneke, J Linzie, B McGlennen, RC
Citation: Kl. Margolis et al., Are benign cellular changes on a Papanicolaou smear really benign? A prospective cohort study, ARCH FAM M, 8(5), 1999, pp. 433-439
Expansion of a 27 CAG repeat allele into a symptomatic Huntington disease-producing allele
Authors: Kelly, TE Allinson, P McGlennen, RC Baker, J Bao, YD
Citation: Te. Kelly et al., Expansion of a 27 CAG repeat allele into a symptomatic Huntington disease-producing allele, AM J MED G, 87(1), 1999, pp. 91-92
Analysis of a very large trinucleotide repeat in a patient with juvenile Huntington's disease
Authors: Nance, MA Mathias-Hagen, V Breningstall, G Wick, MJ McGlennen, RC
Citation: Ma. Nance et al., Analysis of a very large trinucleotide repeat in a patient with juvenile Huntington's disease, NEUROLOGY, 52(2), 1999, pp. 392-394
Risultati: 1-11 |