AAAAAA
Results:
1-11
|
Results: 11
Authors:
ANDERSEN PS
LARSEN LA
KANTERS JK
HAVNDRUPP O
BUNDGAARD H
BRANDT NJ
VUUST J
CHRISTIANSEN M
Citation: Ps. Andersen et al., MUTATION DETECTION BY CLEAVASE IN COMBINATION WITH CAPILLARY-ELECTROPHORESIS ANALYSIS - APPLICATION TO MUTATIONS CAUSING HYPERTROPHIC CARDIOMYOPATHY AND LONG-QT SYNDROME, Molecular diagnosis, 3(2), 1998, pp. 105-111
Authors:
KANTERS JK
LARSEN LA
ORHOLM M
AGNER E
ANDERSEN PS
VUUST J
CHRISTIANSEN M
Citation: Jk. Kanters et al., NOVEL DONOR SPLICE-SITE MUTATION IN THE KVLQT1 GENE IS ASSOCIATED WITH LONG QT SYNDROME, Journal of cardiovascular electrophysiology, 9(6), 1998, pp. 620-624
Authors:
GIVAN A
LARSEN LA
LOEWENSCHUSS A
NIELSEN CJ
Citation: A. Givan et al., INFRARED MATRIX-ISOLATION STUDY OF H2SO4 AND ITS COMPLEXES WITH H2O, Journal of the Chemical Society. Faraday transactions, 94(7), 1998, pp. 827-835
Authors:
GIVAN A
LARSEN LA
LOEWENSCHUSS A
NIELSEN CJ
Citation: A. Givan et al., IR-SPECTRUM OF H2SO4 SPECIES TRAPPED IN LOW-TEMPERATURE SOLID CO AND IN CO CONTAINING MATRICES, Journal of the Chemical Society. Faraday transactions (Print), 94(16), 1998, pp. 2277-2286
Authors:
KANTERS JK
LARSEN LA
ANDERSEN PS
VUUST J
CHRISTIANSEN M
Citation: Jk. Kanters et al., A NOVEL MUTATION IN THE KVLQT1 GENE LEADING TO A RELATIVELY BENIGN FORM OF LONG QT SYNDROME, Circulation, 98(17), 1998, pp. 2407-2407
Authors:
ANDERSEN PS
LARSEN LA
HAVNDRUP O
BUNDGAARD H
KJELDSEN K
VUUST J
CHRISTIANSEN M
Citation: Ps. Andersen et al., BETA-MYOSIN HEAVY-CHAIN MUTATIONS IN DANISH PATIENTS SUFFERING FROM HYPERTROPHIC CARDIOMYOPATHY, The American journal of pathology, 153(5), 1998, pp. 18-18
Authors:
LARSEN LA
GRONSKOV K
NORGAARDPEDERSEN B
BRONDUMNIELSEN K
HASHOLT L
VUUST J
Citation: La. Larsen et al., HIGH-THROUGHPUT ANALYSIS OF FRAGILE-X (CGG)(N) ALLELES IN THE NORMAL AND PREMUTATION RANGE BY PCR AMPLIFICATION AND AUTOMATED CAPILLARY ELECTROPHORESIS, Human genetics, 100(5-6), 1997, pp. 564-568
Authors:
ANDERSEN PS
LARSEN LA
BUNDGAARD H
HAVNDRUP O
KANTERS JK
BRANDT NJ
VUUST J
CHRISTIANSEN M
Citation: Ps. Andersen et al., MUTATION DETECTION BY CLEAVASE(R) IN COMBINATION WITH CAPILLARY GEL-ELECTROPHORESIS - APPLICATION TO MUTATIONS CAUSING HYPERTROPHIC CARDIOMYOPATHY AND LONG QT SYNDROME, The American journal of pathology, 151(5), 1997, pp. 20-20
Authors:
ANDERSEN PS
HAVNDRUP O
BUNDGAARD H
LARSEN LA
KANTERS JK
BRANDT NJ
VUUST J
KJELDSEN K
CHRISTIANSEN M
Citation: Ps. Andersen et al., IDENTIFICATION OF A NOVEL BETA-CARDIAC MYOSIN HEAVY-CHAIN GENE MUTATION THAT CAUSES FAMILIAL HYPERTROPHIC CARDIOMYOPATHY, The American journal of pathology, 151(5), 1997, pp. 21-21
Authors:
LARSEN LA
KANTERS J
ANDERSEN PS
VUUST J
CHRISTIANSEN M
Citation: La. Larsen et al., A METHOD FOR DETECTION OF POINT MUTATIONS IN THE POTASSIUM-CHANNEL ENCODING GENES (KVLQT1 AND HERG) ASSOCIATED WITH LONG-QT SYNDROME AND JERVELL AND LANGE-NIELSEN-SYNDROME, American journal of human genetics, 61(4), 1997, pp. 1290-1290
Authors:
LARSEN LA
CHRISTIANSEN M
NORGAARDPEDERSEN B
VUUST J
Citation: La. Larsen et al., QUANTITATIVE DETECTION OF MALE DNA BY POLYMERASE CHAIN-REACTION USINGA SINGLE PRIMER SET - APPLICATION TO SEX DETERMINATION AND COUNTING OF RARE FETAL CELLS, Analytical biochemistry, 240(1), 1996, pp. 148-150
Risultati:
1-11
|