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                             55 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A competitive allele-specific oligomers polymerase chain reaction assay for the cis double mutation in AMPD1 that is the major cause of myo-adenylate deaminase deficiency Fishbein, William N.
1997
2 p. 121-128
8 p.
artikel
2 An automated semiquantitative B and T cell clonality assay Miller, Jeffrey E.
1999
2 p. 101-117
17 p.
artikel
3 A PCR assay for detecting clonal rearrangement of the TCR-[gamma ] gene Lamberson, Celeste
2001
2 p. 117-124
8 p.
artikel
4 Assessing clinical utility of hepatitis c virus quantitative rt-PCR data: Implications for identification of responders among alpha-interferon-treated patients Ferreira-Gonzalez, A
1996
2 p. 109-120
12 p.
artikel
5 Characterization of RNA in cytologic samples preserved in a methanol-based collection solution Dimulescu, Irina
1998
2 p. 67-72
6 p.
artikel
6 Chromosomal aneuploidy in leukemic blast crisis: A potential source of error in interpretation of bone marrow engraftment analysis by VNTR amplification Zhou, Ming
1999
2 p. 153-157
5 p.
artikel
7 Chronic fatigue syndrome is not associated with expression of endogenous retroviral p15E Gelman, Irwin H.
2000
2 p. 155-156
2 p.
artikel
8 Clinical news update Press, Richard
1999
2 p. 163-165
3 p.
artikel
9 Clinical news update Farkas, Daniel H.
1997
2 p. 157-159
3 p.
artikel
10 Commentary: Molecular detection of breast cancer markers Verbanac, Kathryn M.
2001
2 p. 73-77
5 p.
artikel
11 Comparative evaluation of cleavase fragment length polymorphism with PCR-SSCP and PCR-RFLP to detect antimicrobial agent resistance in Mycobacterium tuberculosis Sreevatsan, Srinand
1998
2 p. 81-91
11 p.
artikel
12 Comparison of two nonradioactive, single-strand conformation polymorphism electrophoretic methods for identification of rpoB mutations in rifampin-resistant isolates of Mycobacterium tuberculosis Cooksey, Robert C.
1998
2 p. 73-80
8 p.
artikel
13 Culture-independent prediction of isoniazid resistance in Mycobacterium tuberculosis by katG gene analysis directly from sputum samples Rinder, Heinz
1999
2 p. 145-152
8 p.
artikel
14 Detection of a novel truncated WT1 transcript in human neoplasia Dechsukhum, Chavaboon
2000
2 p. 117-128
12 p.
artikel
15 Detection of clonal rearrangement of the t-cell receptor gamma gene by polymerase chain reaction and single-strand conformation polymorphism (PCR-SSCP) Kaul, K
1996
2 p. 131-137
7 p.
artikel
16 Development of an internal restriction control in the PCR detection of the methylenetetrahydrofolate reductase (MTHFR) C677T mutation Dubreuil Lastrucci, Rusla M.
1999
2 p. 159-161
3 p.
artikel
17 Diagnostic value of PCR for detection of borrelia burgdorferi DNA in clinical specimens from patients with erythema migrans and lyme neuroborreliosis Lebech, Anne-Mette
2000
2 p. 139-150
12 p.
artikel
18 Efficient recovery of DNA from peripheral blood for diagnostic analysis with a vacuum manifold Kukuczka, Sara M.
2000
2 p. 151-154
4 p.
artikel
19 Enhanced reverse transcriptase polymerase chain reaction for prostate-specific antigen combined with needle biopsy results: A superior predictor of pT3 disease Rubin, Mark A.
1997
2 p. 135-145
11 p.
artikel
20 Enhanced sensitivity with a novel TCRγ PCR assay for clonality studies in 569 formalin-fixed, paraffin-embedded (FFPE) cases Krafft, Amy E.
1999
2 p. 119-133
15 p.
artikel
21 Evaluating children in the Ukraine for colonization with the intestinal bacterium Oxalobacter formigenes, using a polymerase chain reaction-based detection system Sidhu, Harmeet
1997
2 p. 89-97
9 p.
artikel
22 Evaluation of chimerism in DNA samples by PCR amplification of D1S80 with detection by capillary electrophoresis Jone, Cyrenius M.
2000
2 p. 101-105
5 p.
artikel
23 Expression of the cell adhesion molecule CD44 in human lung tumors and cell lines Resnick, Nicole M.
1998
2 p. 93-103
11 p.
artikel
24 Extraskeletal and skeletal myxoid chondrosarcoma: A multiparameter analysis of three cases including cytogenetic analysis and fluorescence in situ hybridization Rao, UN
1996
2 p. 99-107
9 p.
artikel
25 Gene therapy monitoring: Clinical monitoring for efficacy and potential toxicity Hess, Patrick
1997
2 p. 147-155
9 p.
artikel
26 Genetic testing for Ataxia in north america Potter, Nicholas T.
2000
2 p. 91-99
9 p.
artikel
27 Improved detection of viral RNA isolated from liquid-based cytology samples Tarkowski, Trudee A.
2001
2 p. 125-130
6 p.
artikel
28 Letter to the editor Shrimpton, Antony E.
1997
2 p. 160-
1 p.
artikel
29 Molecular cytogenetic analysis of glial tumors using spectral karyotyping and comparative genomic hybridization Squire, Jeremy A.
2001
2 p. 93-108
16 p.
artikel
30 Molecular diagnostics in pediatric acute lymphoblastic leukemia Okuda, T
1996
2 p. 139-151
13 p.
artikel
31 Mthfr (C677T) polymorphisms and stage III colon cancer: Response to therapy Wisotzkey, Jeffrey D.
1999
2 p. 95-99
5 p.
artikel
32 Multidrug resistance in human tumors—molecular diagnosis and clinical significance Ramachandran, Cheppail
1999
2 p. 81-94
14 p.
artikel
33 Mutation detection by cleavase in combination with capillary electrophoresis analysis: Application to mutations causing hypertrophic cardiomyopathy and long-QT syndrome Andersen, Paal Skytt
1998
2 p. 105-111
7 p.
artikel
34 Non-PCR-dependent detection of the factor V leiden mutation from genomic DNA using a homogeneous invader microtiter plate assay Ryan, Daniel
1999
2 p. 135-144
10 p.
artikel
35 Novel chemiluminescent substrate and probe systems for the identification of CFΔF508 genotypes Reddy, Lekkala V.
1997
2 p. 113-120
8 p.
artikel
36 Novel mitochondrial DNA variant that may give a false positive diagnosis for the T8993C mutation White, Sarah L.
1998
2 p. 113-117
5 p.
artikel
37 Pleomorphic (giant and/or spindle cell) carcinoma of lung shows a high percentage of variant CYP1A1*2 Przygodzki, Ronald M.
2001
2 p. 109-115
7 p.
artikel
38 Preliminary draft recommendations from the Secretary's Advisory Committee on Genetic Testing 2000
2 p. 157-158
2 p.
artikel
39 President Clinton signs executive order prohibiting genetic discrimination 2000
2 p. 157-
1 p.
artikel
40 Pushing the envelope of health care Cooper, David L.
1998
2 p. 65-66
2 p.
artikel
41 Quantitative evaluation of post—bone marrow transplant engraftment status using fluorescent-labeled variable number of tandem repeats Luhm, Robert A.
2000
2 p. 129-138
10 p.
artikel
42 Ramification amplification: A novel isothermal DNA amplification method Zhang, David Y.
2001
2 p. 141-150
10 p.
artikel
43 Relationship of p53 genotype to second-look recurrence and survival in ovarian epithelial malignancy Kanbour-Shakir, A
1996
2 p. 121-129
9 p.
artikel
44 Sequence-specific priming and exonuclease-released fluorescence assay for rapid and reliable HLA-A molecular typing Menon, Rajasree
1997
2 p. 99-111
13 p.
artikel
45 Simultaneous detection of C282Y and H63D hemochromatosis mutations by dual-color probes Phillips, Marec
2000
2 p. 107-116
10 p.
artikel
46 Solid-phase amplification and detection: A single-tube diagnostic assay for infectious agents Somodevilla-Torres, Maria
2001
2 p. 131-136
6 p.
artikel
47 Strategies for unambiguous detection of allelic heterozygosity via direct dna sequencing of PCR products: Application to the hla drb1 locus Wu, J
1996
2 p. 89-98
10 p.
artikel
48 The human genome project: A generation's psyche and a society's revolution Cooper, David L.
2000
2 p. 87-89
3 p.
artikel
49 The importance of heteroduplexes in interpreting the results of PCR-RED diagnostic assays: Application to the analysis of mutations in the steroid 21-hydroxylase gene in a case of congenital adrenal hyperplasia Bradley, John F.
1998
2 p. 119-124
6 p.
artikel
50 The issues change. It's the nature of science Cooper, David L.
1999
2 p. 77-80
4 p.
artikel
51 The present and future of molecular diagnostics Leonard, Debra G.B.
2001
2 p. 71-72
2 p.
artikel
52 Thrombophilic mutations impart a high risk of pregnancy-related venous thrombosis 2000
2 p. 158-
1 p.
artikel
53 Transcriptional complementarity in breast cancer: Application to detection of circulating tumor cells Houghton, Raymond L.
2001
2 p. 79-91
13 p.
artikel
54 Two novel mutations in the cystathionine β-synthase gene of homocystinuric patients Tsai, Michael Y.
1997
2 p. 129-133
5 p.
artikel
55 Two rare confounding polymorphisms proximal to the factor V Leiden mutation Gold, Bert
2001
2 p. 137-140
4 p.
artikel
                             55 gevonden resultaten
 
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