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Results:
1-18
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Results: 18
Authors:
Larsen, LA
Johnson, M
Brown, C
Christiansen, M
Frank-Hansen, R
Vuust, J
Andersen, PS
Citation: La. Larsen et al., Automated mutation screening using dideoxy fingerprinting and capillary array electrophoresis, HUM MUTAT, 18(5), 2001, pp. 451-457
Authors:
Larsen, LA
Vuust, J
Nystad, M
Evseeva, I
Van Ghelue, M
Tranebjaerg, L
Citation: La. Larsen et al., Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with Asia, EUR J HUM G, 9(9), 2001, pp. 724-727
Authors:
Tyson, J
Tranebjaerg, L
McEntagart, M
Larsen, LA
Christiansen, M
Whiteford, ML
Bathen, J
Aslaksen, B
Sorland, SJ
Lund, O
Pembrey, ME
Malcolm, S
Bitner-Glindzicz, M
Citation: J. Tyson et al., Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen (vol 107, pg 499, 2000), HUM GENET, 108(1), 2001, pp. 75-75
Authors:
Larsen, LA
Andersen, PS
Kanters, J
Svendsen, IH
Jacobsen, JR
Vuust, J
Wettrell, G
Tranebjaerg, L
Bathen, J
Christiansen, M
Citation: La. Larsen et al., Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRPI ion channel: Implications for acquired and congenital long Q-T syndrome, CLIN CHEM, 47(8), 2001, pp. 1390-1395
Authors:
Havndrup, O
Bundgaard, H
Andersen, PS
Larsen, LA
Vuust, J
Kjeldsen, K
Christiansen, M
Citation: O. Havndrup et al., The Val(606)Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death af young age, AM J CARD, 87(11), 2001, pp. 1315-1317
Authors:
Havndrup, O
Bundgaard, H
Andersen, PS
Larsen, LA
Vuust, J
Kjeldsen, K
Christiansen, M
Citation: O. Havndrup et al., A novel missense mutation, Leu390Val, in the cardiac ss-myosin heavy chainassociated with pronounced septal hypertrophy in two families with hypertrophic cardiomyopathy, SC CARDIOVA, 34(6), 2000, pp. 558-563
Authors:
Larsen, LA
Christiansen, M
Vuust, J
Andersen, PS
Citation: La. Larsen et al., High throughput mutation screening by automated capillary electrophoresis, COMB CHEM H, 3(5), 2000, pp. 393-409
Authors:
Milne, RW
Larsen, LA
Jorgensen, KL
Bastlund, J
Stretch, GR
Evans, AM
Citation: Rw. Milne et al., Hepatic disposition of fexofenadine: Influence of the transport inhibitorserythromycin and dibromosulphothalein, PHARM RES, 17(12), 2000, pp. 1511-1515
Authors:
Tyson, J
Tranebjaerg, L
McEntagart, M
Larsen, LA
Christiansen, M
Whiteford, ML
Bathen, J
Aslaksen, B
Sorland, SJ
Lund, O
Pembrey, ME
Malcolm, S
Bitner-Glindzicz, M
Citation: J. Tyson et al., Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-Nielsen, HUM GENET, 107(5), 2000, pp. 499-503
Authors:
Larsen, LA
Armstrong, JSM
Gronskov, K
Hjalgrim, H
Macpherson, JN
Brondum-Nielsen, K
Hasholt, L
Norgaard-Pedersen, B
Vuust, J
Citation: La. Larsen et al., Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: Implications for multiple mutational pathways towards fragile X alleles, AM J MED G, 93(2), 2000, pp. 99-106
Authors:
Larsen, LA
Svendsen, IH
Jensen, AM
Kanters, JK
Andersen, PS
Moller, M
Sorensen, SA
Sandoe, E
Jacobsen, JR
Vuust, J
Christiansen, M
Citation: La. Larsen et al., Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2, CLIN GENET, 57(2), 2000, pp. 125-130
Authors:
Larsen, LA
Christiansen, M
Vuust, J
Andersen, PS
Citation: La. Larsen et al., High-throughput single-strand conformation polymorphism analysis by automated capillary electrophoresis: Robust multiplex analysis and pattern-based identification of allelic variants, HUM MUTAT, 13(4), 1999, pp. 318-327
Authors:
Larsen, LA
Armstrong, JSM
Gronskov, K
Hjalgrim, H
Brondum-Nielsen, K
Hasholt, L
Norgaard-Pedersen, B
Vuust, J
Citation: La. Larsen et al., Analysis of FMR1 (CGG)(n) alleles and FRAXA microsatellite haplotypes in the population of Greenland: implications for the population of the New World from Asia, EUR J HUM G, 7(7), 1999, pp. 771-777
Authors:
Larsen, LA
Fosdal, I
Andersen, PS
Kanters, JK
Vuust, J
Wettrell, G
Christiansen, M
Citation: La. Larsen et al., Recessive Romano-Ward syndrome associated with compound heterozygosity fortwo mutations in the KVLQT1 gene, EUR J HUM G, 7(6), 1999, pp. 724-728
Authors:
Givan, A
Larsen, LA
Loewenschuss, A
Nielsen, CJ
Citation: A. Givan et al., Matrix isolation mid- and far-infrared spectra of sulfuric acid and deuterated sulfuric acid vapors, J MOL STRUC, 509(1-3), 1999, pp. 35-47
Authors:
Bundgaard, H
Havndrup, O
Andersen, PS
Larsen, LA
Brandt, NJ
Vuust, J
Kjeldsen, K
Christiansen, M
Citation: H. Bundgaard et al., Familial hypertrophic cardiomyopathy associated with a novel missense mutation affecting the ATP-binding region of the cardiac beta-myosin heavy chain, J MOL CEL C, 31(4), 1999, pp. 745-750
Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 gene
Authors:
Andersen, PS
Havndrup, O
Bundgaard, H
Larsen, LA
Vuust, J
Kjeldsen, K
Christiansen, M
Citation: Ps. Andersen et al., Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 gene, CLIN GENET, 56(3), 1999, pp. 244-246
Authors:
Larsen, LA
Andersen, PS
Kanters, JK
Jacobsen, JR
Vuust, J
Christiansen, M
Citation: La. Larsen et al., A single strand conformation polymorphism heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome, CLIN CHIM A, 280(1-2), 1999, pp. 113-125
Risultati:
1-18
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