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Zeitschrift Fur Kardiologie
|
May 16, 2000
Molecular genetics of arrhythmias--a new paradigm
E Schulze-Bahr, W Haverkamp, M Borggrefe, et al.
Human Genetics
|
October 28, 1997
Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneous
E Schulze-Bahr, W Haverkamp, H Wedekind, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
November 1, 1995
Molecular analysis at the Harvey Ras-1 gene in patients with long QT syndrome
E Schulze-Bahr, W Haverkamp, H Wiebusch, et al.
Nucleic Acids Research
|
February 11, 1987
Human apolipoprotein CI (ApoC1) gene locus: BglI dimorphic site
P M Frossard, D W Lim, R T Coleman, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
July 1, 1997
Evidence of alternative promoters directing isoform-specific expression of human endothelin-converting enzyme-1 mRNA in cultured endothelial cells
H D Orzechowski, C M Richter, H Funke-Kaiser, et al.
Journal of Neurology
|
July 5, 2001
Mutation analysis in Chariot-Marie Tooth disease type 1: point mutations in the MPZ gene and the GJB1 gene cause comparable phenotypic heterogeneity
P Young, K Grote, G Kuhlenbäumer, et al.
Circulation
|
October 1, 1996
Compound heterozygosity for a structural apolipoprotein A-I variant, apo A-I(L141R)Pisa, and an apolipoprotein A-I null allele in patients with absence of HDL cholesterol, corneal opacifications, and coronary heart disease
R Miccoli, A Bertolotto, R Navalesi, et al.
Human Genetics
|
February 1, 1996
A missense mutation (Thr-6Pro) in the lysosomal acid lipase (LAL) gene is present with a high frequency in three different ethnic populations: impact on serum lipoprotein concentrations
S Muntoni, H Wiebusch, H Funke, et al.
Neurology
|
April 1, 1998
PCR-based strategy for the diagnosis of hereditary neuropathy with liability to pressure palsies and Charcot-Marie-Tooth disease type 1A
P Young, F Stögbauer, H Wiebusch, et al.
The Journal of Molecular Diagnostics : JMD
|
September 19, 2016
Multiplexed Reference Materials as Controls for Diagnostic Next-Generation Sequencing: A Pilot Investigating Applications for Hypertrophic Cardiomyopathy
Emily M Kudalkar, Naif A M Almontashiri, Catherine Huang, et al.
Page
of 21
Search research articles
Search
Showing results (121-130 of 203) with videos related to
Sort By:
Page
of 21
Zeitschrift Fur Kardiologie
|
May 16, 2000
Molecular genetics of arrhythmias--a new paradigm
E Schulze-Bahr, W Haverkamp, M Borggrefe, et al.
Human Genetics
|
October 28, 1997
Autosomal recessive long-QT syndrome (Jervell Lange-Nielsen syndrome) is genetically heterogeneous
E Schulze-Bahr, W Haverkamp, H Wedekind, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
November 1, 1995
Molecular analysis at the Harvey Ras-1 gene in patients with long QT syndrome
E Schulze-Bahr, W Haverkamp, H Wiebusch, et al.
Nucleic Acids Research
|
February 11, 1987
Human apolipoprotein CI (ApoC1) gene locus: BglI dimorphic site
P M Frossard, D W Lim, R T Coleman, et al.
Journal of Molecular Medicine (Berlin, Germany)
|
July 1, 1997
Evidence of alternative promoters directing isoform-specific expression of human endothelin-converting enzyme-1 mRNA in cultured endothelial cells
H D Orzechowski, C M Richter, H Funke-Kaiser, et al.
Journal of Neurology
|
July 5, 2001
Mutation analysis in Chariot-Marie Tooth disease type 1: point mutations in the MPZ gene and the GJB1 gene cause comparable phenotypic heterogeneity
P Young, K Grote, G Kuhlenbäumer, et al.
Circulation
|
October 1, 1996
Compound heterozygosity for a structural apolipoprotein A-I variant, apo A-I(L141R)Pisa, and an apolipoprotein A-I null allele in patients with absence of HDL cholesterol, corneal opacifications, and coronary heart disease
R Miccoli, A Bertolotto, R Navalesi, et al.
Human Genetics
|
February 1, 1996
A missense mutation (Thr-6Pro) in the lysosomal acid lipase (LAL) gene is present with a high frequency in three different ethnic populations: impact on serum lipoprotein concentrations
S Muntoni, H Wiebusch, H Funke, et al.
Neurology
|
April 1, 1998
PCR-based strategy for the diagnosis of hereditary neuropathy with liability to pressure palsies and Charcot-Marie-Tooth disease type 1A
P Young, F Stögbauer, H Wiebusch, et al.
The Journal of Molecular Diagnostics : JMD
|
September 19, 2016
Multiplexed Reference Materials as Controls for Diagnostic Next-Generation Sequencing: A Pilot Investigating Applications for Hypertrophic Cardiomyopathy
Emily M Kudalkar, Naif A M Almontashiri, Catherine Huang, et al.
Page
of 21