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Results of search for 'au:"Syvanen, A C"', page 4 of 6
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Authors
Aalto-Setälä, K
Aula, P
Barbany, G
Bengtström, M
Eloranta, M-L
Grön, K
Halila, R
Hamberg, U
Ikonen, E
Kontula, K
Lindroos, K
Lukka, M
Palotie, A
Paunio, T
Peltonen, L
Sajantila, A
Suomalainen, A
Syvänen, A C
Syvänen, A-C
Söderlund, H
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Animals
Base Sequence
DNA
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Gene Frequency
Genotype
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Molecular Sequence Data
Polymerase Chain Reaction
Polymorphism, Single Nucleotide
Sequence Analysis, DNA
analysis
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genetics
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Your search returned 114 results.
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61.
Cytomegalovirus in urine: detection of viral DNA by sandwich hybridization.
[electronic resource]
by
Virtanen, M
Syvänen, A C
Oram, J
Söderlund, H
Ranki, M
Producer:
19850306
In:
Journal of clinical microbiology
vol. 20
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62.
Determination of the frequencies of ten allelic variants of the Wilson disease gene (ATP7B), in pooled DNA samples.
[electronic resource]
by
Olsson, C
Waldenström, E
Westermark, K
Landegre, U
Syvänen, A C
Producer:
20010222
In:
European journal of human genetics : EJHG
vol. 8
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63.
An accurate method for comparing transcript levels of two alleles or highly homologous genes: application to fibrillin transcripts in Marfan patients' fibroblasts.
[electronic resource]
by
Karttunen, L
Lönnqvist, L
Godfrey, M
Peltonen, L
Syvänen, A C
Producer:
19961112
In:
Genome research
vol. 6
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64.
Apolipoprotein E polymorphism determined by restriction enzyme analysis of DNA amplified by polymerase chain reaction: convenient alternative to phenotyping by isoelectric focusing.
[electronic resource]
by
Kontula, K
Aalto-Setälä, K
Kuusi, T
Hämäläinen, L
Syvänen, A C
Producer:
19910124
In:
Clinical chemistry
vol. 36
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65.
Quantification of point mutations associated with Leber hereditary optic neuroretinopathy by solid-phase minisequencing.
[electronic resource]
by
Juvonen, V
Huoponen, K
Syvänen, A C
Nikoskelainen, E
Savontaus, M L
Producer:
19940203
In:
Human genetics
vol. 93
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66.
Genetic analysis of the polymorphism of the human apolipoprotein E using automated solid-phase sequencing.
[electronic resource]
by
Syvänen, A C
Hultman, T
Aalto-Setälä, K
Söderlund, H
Uhlén, M
Producer:
19911003
In:
Genetic analysis, techniques and applications
vol. 8
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67.
Amount of introgression in flycatcher hybrid zones reflects regional differences in pre and post-zygotic barriers to gene exchange.
[electronic resource]
by
Borge, T
Lindroos, K
Nádvorník, P
Syvänen, A-C
Saetre, G-P
Producer:
20060615
In:
Journal of evolutionary biology
vol. 18
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68.
A primer-guided nucleotide incorporation assay in the genotyping of apolipoprotein E.
[electronic resource]
by
Syvänen, A C
Aalto-Setälä, K
Harju, L
Kontula, K
Söderlund, H
Producer:
19910305
In:
Genomics
vol. 8
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69.
Quantification of mitochondrial DNA carrying the tRNA(8344Lys) point mutation in myoclonus epilepsy and ragged-red-fiber disease.
[electronic resource]
by
Suomalainen, A
Kollmann, P
Octave, J N
Söderlund, H
Syvänen, A C
Producer:
19940929
In:
European journal of human genetics : EJHG
vol. 1
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70.
DNA-based carrier screening in primary healthcare: screening for aspartylglucosaminuria mutations in maternity health offices.
[electronic resource]
by
Hietala, M
Aula, P
Syvänen, A C
Isoniemi, A
Peltonen, L
Palotie, A
Producer:
19961022
In:
Clinical chemistry
vol. 42
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71.
Assessing hematopoietic chimerism after allogeneic stem cell transplantation by multiplexed SNP genotyping using microarrays and quantitative analysis of SNP alleles.
[electronic resource]
by
Fredriksson, M
Barbany, G
Liljedahl, U
Hermanson, M
Kataja, M
Syvänen, A-C
Producer:
20040224
In:
Leukemia
vol. 18
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72.
Tissue distribution and levels of gelsolin mRNA in normal individuals and patients with gelsolin-related amyloidosis.
[electronic resource]
by
Paunio, T
Kangas, H
Kiuru, S
Palo, J
Peltonen, L
Syvänen, A C
Producer:
19970515
In:
FEBS letters
vol. 406
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73.
Variation in genes in the endothelin pathway and endothelium-dependent and endothelium-independent vasodilation in an elderly population.
[electronic resource]
by
Lind, L
Syvänen, A-C
Axelsson, T
Lundmark, P
Hägg, S
Larsson, A
Producer:
20131017
In:
Acta physiologica (Oxford, England)
vol. 208
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74.
The geographic distribution of monoamine oxidase haplotypes supports a bottleneck during the dispersion of modern humans from Africa.
[electronic resource]
by
Balciuniene, J
Syvänen, A C
McLeod, H L
Pettersson, U
Jazin, E E
Producer:
20010614
In:
Journal of molecular evolution
vol. 52
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75.
N-ras gene mutations in acute myeloid leukemia: accurate detection by solid-phase minisequencing.
[electronic resource]
by
Syvänen, A C
Söderlund, H
Laaksonen, E
Bengtström, M
Turunen, M
Palotie, A
Producer:
19920415
In:
International journal of cancer
vol. 50
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76.
Aspartylglucosaminuria (AGU): protein and gene structure of normal and mutated aspartylglucosaminidase.
[electronic resource]
by
Halila, R
Ikonen, E
Tollersrud, O
Syvänen, A C
Enomaa, N
Peltonen, L
Producer:
19931021
In:
Biochemical medicine and metabolic biology
vol. 50
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77.
A system for specific, high-throughput genotyping by allele-specific primer extension on microarrays.
[electronic resource]
by
Pastinen, T
Raitio, M
Lindroos, K
Tainola, P
Peltonen, L
Syvänen, A C
Producer:
20000928
In:
Genome research
vol. 10
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78.
A chimeric disposition of the elongation factor genes in Rickettsia prowazekii.
[electronic resource]
by
Syvänen, A C
Amiri, H
Jamal, A
Andersson, S G
Kurland, C G
Producer:
19970113
In:
Journal of bacteriology
vol. 178
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79.
Genotypes of catechol-O-methyltransferase and response to levodopa treatment in patients with Parkinson's disease.
[electronic resource]
by
Lee, M S
Lyoo, C H
Ulmanen, I
Syvänen, A C
Rinne, J O
Producer:
20010419
In:
Neuroscience letters
vol. 298
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80.
The level of the mitochondrial mutation A3243G decreases upon ageing in epithelial cells from individuals with diabetes and deafness.
[electronic resource]
by
Olsson, C
Johnsen, E
Nilsson, M
Wilander, E
Syvänen, A C
Lagerström-Fermér, M
Producer:
20020507
In:
European journal of human genetics : EJHG
vol. 9
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