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Journal of Crohn'S & Colitis
|
January 8, 2014
Genetic susceptibility and genotype-phenotype association in 588 Danish children with inflammatory bowel disease
C Jakobsen, I Cleynen, P S Andersen, et al.
Journal of Safety Research
|
November 10, 2010
Improving construction site safety through leader-based verbal safety communication
Pete Kines, Lars P S Andersen, Soren Spangenberg, et al.
Clinical Genetics
|
November 24, 1999
Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 gene
P S Andersen, O Havndrup, H Bundgaard, et al.
The American Journal of Cardiology
|
May 30, 2001
The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age
O Havndrup, H Bundgaard, P S Andersen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 25, 1999
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
L A Larsen, P S Andersen, J K Kanters, et al.
Scandinavian Cardiovascular Journal : SCJ
|
February 24, 2001
A novel missense mutation, Leu390Val, in the cardiac beta-myosin heavy chain associated with pronounced septal hypertrophy in two families with hypertrophic cardiomyopathy
O Havndrup, H Bundgaard, P S Andersen, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology
|
May 10, 2013
Risk factors for Staphylococcus aureus nasal colonization in Danish middle-aged and elderly twins
P S Andersen, L A Larsen, V G Fowler, et al.
The British Journal of Dermatology
|
March 21, 2017
Staphylococcus aureus colonization in atopic eczema and its association with filaggrin gene mutations
M-L Clausen, S M Edslev, P S Andersen, et al.
Journal of Medical Genetics
|
May 19, 2001
Development and application of linkage analysis in genetic diagnosis of familial hypertrophic cardiomyopathy
J Mogensen, P S Andersen, U Steffensen, et al.
Journal of Cardiovascular Electrophysiology
|
July 8, 1998
Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndrome
J K Kanters, L A Larsen, M Orholm, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 71) with videos related to
Sort By:
Page
of 8
Journal of Crohn'S & Colitis
|
January 8, 2014
Genetic susceptibility and genotype-phenotype association in 588 Danish children with inflammatory bowel disease
C Jakobsen, I Cleynen, P S Andersen, et al.
Journal of Safety Research
|
November 10, 2010
Improving construction site safety through leader-based verbal safety communication
Pete Kines, Lars P S Andersen, Soren Spangenberg, et al.
Clinical Genetics
|
November 24, 1999
Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 gene
P S Andersen, O Havndrup, H Bundgaard, et al.
The American Journal of Cardiology
|
May 30, 2001
The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age
O Havndrup, H Bundgaard, P S Andersen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 25, 1999
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
L A Larsen, P S Andersen, J K Kanters, et al.
Scandinavian Cardiovascular Journal : SCJ
|
February 24, 2001
A novel missense mutation, Leu390Val, in the cardiac beta-myosin heavy chain associated with pronounced septal hypertrophy in two families with hypertrophic cardiomyopathy
O Havndrup, H Bundgaard, P S Andersen, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology
|
May 10, 2013
Risk factors for Staphylococcus aureus nasal colonization in Danish middle-aged and elderly twins
P S Andersen, L A Larsen, V G Fowler, et al.
The British Journal of Dermatology
|
March 21, 2017
Staphylococcus aureus colonization in atopic eczema and its association with filaggrin gene mutations
M-L Clausen, S M Edslev, P S Andersen, et al.
Journal of Medical Genetics
|
May 19, 2001
Development and application of linkage analysis in genetic diagnosis of familial hypertrophic cardiomyopathy
J Mogensen, P S Andersen, U Steffensen, et al.
Journal of Cardiovascular Electrophysiology
|
July 8, 1998
Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndrome
J K Kanters, L A Larsen, M Orholm, et al.
Page
of 8