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Cytogenetics and Cell Genetics
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June 1, 2000
Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumors
M J Steenman, N Zijlstra, D L Kruitbosch, et al.
Cytogenetics and Cell Genetics
|
January 1, 1989
Assignment of the gene coding for human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to chromosome region 3p22----p23
A Bout, J M Hoovers, E Bakker, et al.
The Journal of Biological Chemistry
|
September 25, 1998
The human chitotriosidase gene. Nature of inherited enzyme deficiency
R G Boot, G H Renkema, M Verhoek, et al.
Clinical Genetics
|
March 29, 2000
Molecular genetic testing for familial hypercholesterolemia: spectrum of LDL receptor gene mutations in The Netherlands
M P Lombardi, E J Redeker, J C Defesche, et al.
Nature Genetics
|
September 2, 1999
Cardiac conduction defects associate with mutations in SCN5A
J J Schott, C Alshinawi, F Kyndt, et al.
Cardiovascular Research
|
February 26, 2000
Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome
M B Rook, C Bezzina Alshinawi, W A Groenewegen, et al.
Human Mutation
|
January 1, 1997
Glucocerebrosidase genotype of Gaucher patients in The Netherlands: limitations in prognostic value
R G Boot, C E Hollak, M Verhoek, et al.
Human Mutation
|
April 8, 2011
Mutation update for the PORCN gene
Maria Paola Lombardi, Saskia Bulk, Jacopo Celli, et al.
Atherosclerosis
|
October 10, 2008
Low HDL cholesterol levels in type I Gaucher disease do not lead to an increased risk of cardiovascular disease
M de Fost, M Langeveld, R Franssen, et al.
Atherosclerosis
|
May 11, 2013
A novel lamin A/C mutation in a Dutch family with premature atherosclerosis
A A W Weterings, I A W van Rijsingen, A S Plomp, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 22) with videos related to
Sort By:
Page
of 3
Cytogenetics and Cell Genetics
|
June 1, 2000
Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumors
M J Steenman, N Zijlstra, D L Kruitbosch, et al.
Cytogenetics and Cell Genetics
|
January 1, 1989
Assignment of the gene coding for human peroxisomal 3-oxoacyl-CoA thiolase (ACAA) to chromosome region 3p22----p23
A Bout, J M Hoovers, E Bakker, et al.
The Journal of Biological Chemistry
|
September 25, 1998
The human chitotriosidase gene. Nature of inherited enzyme deficiency
R G Boot, G H Renkema, M Verhoek, et al.
Clinical Genetics
|
March 29, 2000
Molecular genetic testing for familial hypercholesterolemia: spectrum of LDL receptor gene mutations in The Netherlands
M P Lombardi, E J Redeker, J C Defesche, et al.
Nature Genetics
|
September 2, 1999
Cardiac conduction defects associate with mutations in SCN5A
J J Schott, C Alshinawi, F Kyndt, et al.
Cardiovascular Research
|
February 26, 2000
Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome
M B Rook, C Bezzina Alshinawi, W A Groenewegen, et al.
Human Mutation
|
January 1, 1997
Glucocerebrosidase genotype of Gaucher patients in The Netherlands: limitations in prognostic value
R G Boot, C E Hollak, M Verhoek, et al.
Human Mutation
|
April 8, 2011
Mutation update for the PORCN gene
Maria Paola Lombardi, Saskia Bulk, Jacopo Celli, et al.
Atherosclerosis
|
October 10, 2008
Low HDL cholesterol levels in type I Gaucher disease do not lead to an increased risk of cardiovascular disease
M de Fost, M Langeveld, R Franssen, et al.
Atherosclerosis
|
May 11, 2013
A novel lamin A/C mutation in a Dutch family with premature atherosclerosis
A A W Weterings, I A W van Rijsingen, A S Plomp, et al.
Page
of 3