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Results:
1-7
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Results: 7
Authors:
Rhodes, RB
Lewis, K
Shultz, J
Huber, S
Voelkerding, KV
Leonard, DGB
Tsongalis, GJ
Kephart, DD
Citation: Rb. Rhodes et al., Analysis of the factor V Leiden mutation using the READIT Assay, MOL DIAGN, 6(1), 2001, pp. 55-61
Authors:
Hessner, MJ
Friedman, KD
Voelkerding, KV
Huber, S
Ryan, D
Nuccie, B
Ledford, M
Citation: Mj. Hessner et al., Multisite study for genotyping of the factor II (prothrombin) G20210A mutation by the invader assay, CLIN CHEM, 47(11), 2001, pp. 2048-2050
Authors:
Huber, S
McMaster, KJ
Voelkerding, KV
Citation: S. Huber et al., Analytical evaluation of primer engineered multiplex polymerase chain reaction-restriction fragment length polymorphism for detection of factor V Leiden and prothrombin G20210A, J MOL DIAGN, 2(3), 2000, pp. 153-157
Authors:
Voelkerding, KV
Citation: Kv. Voelkerding, Finding a workable balance - Regulation of genetic testing in the human genome era, J MOL DIAGN, 2(2), 2000, pp. 57-59
Authors:
Huber, S
Voelkerding, KV
Citation: S. Huber et Kv. Voelkerding, Molecular diagnosis of hereditary hemochromatosis, METH MOL M, 49, 2000, pp. 439-450
Authors:
Carrel, AL
Huber, S
Allen, DB
Voelkerding, KV
Citation: Al. Carrel et al., Assessment of SNRPN expression as a molecular tool in the diagnosis of Prader-Willi syndrome, MOL DIAGN, 4(1), 1999, pp. 5-10
Authors:
Strobl, FJ
Voelkerding, KV
Smith, EP
Citation: Fj. Strobl et al., Management of chronic myeloid leukemia during pregnancy with leukapheresis, J CLIN APH, 14(1), 1999, pp. 42-44
Risultati:
1-7
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