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Results: 1-10 |
Results: 10
An overview of molecular diagnosis of steroid 21-hydroxylase deficiency
Authors: Keegan, CE Killeen, AA
Citation: Ce. Keegan et Aa. Killeen, An overview of molecular diagnosis of steroid 21-hydroxylase deficiency, J MOL DIAGN, 3(2), 2001, pp. 49-54
Molecular analysis of congenital adrenal hyperplasia in a newborn screening program
Authors: Killeen, AA
Citation: Aa. Killeen, Molecular analysis of congenital adrenal hyperplasia in a newborn screening program, MOL DIAGN, 6(3), 2001, pp. 189-191
Association of the prothrombin G20210A mutation with factor V Leiden in a Midwestern American population
Authors: Bavikatty, NR Killeen, AA Akel, N Normolle, D Schmaier, AH
Citation: Nr. Bavikatty et al., Association of the prothrombin G20210A mutation with factor V Leiden in a Midwestern American population, AM J CLIN P, 114(2), 2000, pp. 272-275
Evaluation of chimerism in DNA samples by PCR amplification of D1S80 with detection by capillary electrophoresis
Authors: Jone, CM Akel, N Killeen, AA
Citation: Cm. Jone et al., Evaluation of chimerism in DNA samples by PCR amplification of D1S80 with detection by capillary electrophoresis, MOL DIAGN, 5(2), 2000, pp. 101-105
Analysis of CYP21 coding polymorphisms in three ethnic populations: Further evidence of nonamplifying CYP21 alleles among whites
Authors: Ozturk, IC Wei, WL Palaniappan, L Rubenfire, M Killeen, AA
Citation: Ic. Ozturk et al., Analysis of CYP21 coding polymorphisms in three ethnic populations: Further evidence of nonamplifying CYP21 alleles among whites, MOL DIAGN, 5(1), 2000, pp. 47-52
Genotyping of apolipoprotein E
Authors: Ozturk, IC Akel, N Killeen, AA
Citation: Ic. Ozturk et al., Genotyping of apolipoprotein E, METH MOL M, 49, 2000, pp. 451-457
Chromosomal aneuploidy in leukemic blast crisis: A potential source of error in interpretation of bone marrow engraftment analysis by VNTR amplification
Authors: Zhou, M Sheldon, S Akel, N Killeen, AA
Citation: M. Zhou et al., Chromosomal aneuploidy in leukemic blast crisis: A potential source of error in interpretation of bone marrow engraftment analysis by VNTR amplification, MOL DIAGN, 4(2), 1999, pp. 153-157
Single-nucleotide polymorphisms in intron 2 of CYPZ1P: Evidence for a higher rate of mutation at CpG dinucleotides in the functional steroid 21-hydroxylase gene and application to segregation analysis in congenital adrenal hyperplasia
Authors: Jiddou, RR Wei, WL Sane, KS Killeen, AA
Citation: Rr. Jiddou et al., Single-nucleotide polymorphisms in intron 2 of CYPZ1P: Evidence for a higher rate of mutation at CpG dinucleotides in the functional steroid 21-hydroxylase gene and application to segregation analysis in congenital adrenal hyperplasia, CLIN CHEM, 45(5), 1999, pp. 625-629
An overview of genetic factors influencing plasma lipid levels and coronary artery disease risk
Authors: Ozturk, IC Killeen, AA
Citation: Ic. Ozturk et Aa. Killeen, An overview of genetic factors influencing plasma lipid levels and coronary artery disease risk, ARCH PATH L, 123(12), 1999, pp. 1219-1222
Characterization of frequent polymorphisms in intron 2 of CYP21: application to analysis of segregation of CYP21 alleles
Authors: Killeen, AA Jiddou, RR Sane, KS
Citation: Aa. Killeen et al., Characterization of frequent polymorphisms in intron 2 of CYP21: application to analysis of segregation of CYP21 alleles, CLIN CHEM, 44(12), 1998, pp. 2410-2415
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