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Results: 1-8 |
Results: 8
Quality control in molecular genetic testing
Authors: Dequeker, E Ramsden, S Grody, WW Stenzel, TT Barton, DE
Citation: E. Dequeker et al., Quality control in molecular genetic testing, NAT REV GEN, 2(9), 2001, pp. 717-723
Fluorescent, multiplexed, automated, primer-extension assay for 3120+1G ->A and I148T mutations in cystic fibrosis
Authors: Brown, NM Bernacki, S Pratt, VM Stenzel, TT
Citation: Nm. Brown et al., Fluorescent, multiplexed, automated, primer-extension assay for 3120+1G ->A and I148T mutations in cystic fibrosis, CLIN CHEM, 47(11), 2001, pp. 2053-2055
Successful allogeneic engraftment of mismatched unrelated cord blood following a nonmyeloablative preparative regimen
Authors: Rizzieri, DA Long, GD Vredenburgh, JJ Gasparetto, C Morris, A Stenzel, TT Davis, P Chao, NJ
Citation: Da. Rizzieri et al., Successful allogeneic engraftment of mismatched unrelated cord blood following a nonmyeloablative preparative regimen, BLOOD, 98(12), 2001, pp. 3486-3488
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
The pathology of liver-localized post-transplant lymphoproliferative disease - A report of three cases and a review of the literature
Authors: Nuckols, JD Baron, PW Stenzel, TT Olatidoye, BA Tuttle-Newhall, JE Clavien, PA Howell, DN
Citation: Jd. Nuckols et al., The pathology of liver-localized post-transplant lymphoproliferative disease - A report of three cases and a review of the literature, AM J SURG P, 24(5), 2000, pp. 733-741
Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results
Authors: Noll, WW Belloni, DR Stenzel, TT Grody, WW
Citation: Ww. Noll et al., Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results, NAT GENET, 23(3), 1999, pp. 271-272
Translocation (15;17)(q22;q21) as a secondary chromosomal abnormality in acase of acute monoblastic leukemia with tetrasomy 8
Authors: Zhang, XX Robinson, LJ Stenzel, TT Qumsiyeh, MB
Citation: Xx. Zhang et al., Translocation (15;17)(q22;q21) as a secondary chromosomal abnormality in acase of acute monoblastic leukemia with tetrasomy 8, CANC GENET, 113(1), 1999, pp. 9-13
Molecular genetic aspects of oligodendrogliomas including analysis by comparative genomic hybridization
Authors: Bigner, SH Matthews, MR Rasheed, BKA Wiltshire, RN Friedman, HS Friedman, AH Stenzel, TT Dawes, DM McLendon, RE Bigner, DD
Citation: Sh. Bigner et al., Molecular genetic aspects of oligodendrogliomas including analysis by comparative genomic hybridization, AM J PATH, 155(2), 1999, pp. 375-386
Risultati: 1-8 |