Lars Allan Larsen
curis.ku.dk
0000-0002-7536-1172
Københavns Universitet
88 papers found
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Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 gene
Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene
Familial Hypertrophic Cardiomyopathy Associated with a Novel Missense Mutation Affecting the ATP-binding Region of the Cardiac Beta-myosin Heavy Chain
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
Mutation detection by cleavase in combination with capillary electrophoresis analysis: Application to mutations causing hypertrophic cardiomyopathy and long-QT syndrome*
Novel Donor Splice Site Mutation in the KVLQT1 Gene is Associated with Long QT Syndrome
High-throughput analysis of Fragile X (CGG) n alleles in the normal and premutation range by PCR amplification and automated capillary electrophoresis
Quantitative Detection of Male DNA by Polymerase Chain Reaction Using a Single Primer Set: Application to Sex Determination and Counting of Rare Fetal Cells
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