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I N Day

Showing results (61-70 of 80) with videos related to

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Stroke|September 8, 2001
Polymorphisms in matrix metalloproteinase-1, -3, -9, and -12 genes in relation to subarachnoid hemorrhageB Zhang, S Dhillon, I Geary, et al.
Journal of Lipid Research|June 5, 1999
Evidence for a third genetic locus causing familial hypercholesterolemia. A non-LDLR, non-APOB kindredL Haddad, I N Day, S Hunt, et al.
Clinical Genetics|July 11, 1998
Applicability of LDLR flanking microsatellite polymorphisms for prenatal diagnosis of homozygous state for familial hypercholesterolemiaE R De Oliveira e Silva, L Haddad, P O Kwiterovich, et al.
Journal of Medical Genetics|February 1, 1997
Identification of a common low density lipoprotein receptor mutation (R329X) in the south of England: complete linkage disequilibrium with an allele of microsatellite D19S394I N Day, L Haddad, S D O'Dell, et al.
Annals of Human Genetics|October 1, 1991
The gene for human neurone specific ubiquitin C-terminal hydrolase (UCHL1, PGP9.5) maps to chromosome 4p14Y H Edwards, M F Fox, S Povey, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|May 13, 1998
W64R mutation in beta-3-adrenergic receptor gene and weight in a large population sampleS D O'Dell, M K Bolla, G J Miller, et al.
Thrombosis and Haemostasis|December 22, 1999
Gene-environment interaction in the determination of levels of plasma fibrinogenS E Humphries, L A Luong, H E Montgomery, et al.
Human Mutation|January 1, 1997
Spectrum of LDL receptor gene mutations in heterozygous familial hypercholesterolemiaI N Day, R A Whittall, S D O'Dell, et al.
Human Mutation|January 1, 1997
A high incidence of mutations in exon 6 of the low-density lipoprotein receptor gene in Greek familial hypercholesterolemia patients, including a novel mutationN Mavroidis, J Traeger-Synodinos, E Kanavakis, et al.
Human Genetics|April 17, 1998
Analysis of low density lipoprotein receptor gene mutations and microsatellite haplotypes in Greek FH heterozygous children: six independent ancestors account for 60% of probandsJ Traeger-Synodinos, N Mavroidis, E Kanavakis, et al.
Pageof 8

Showing results (61-70 of 80) with videos related to

Sort By:
Pageof 8
Stroke|September 8, 2001
Polymorphisms in matrix metalloproteinase-1, -3, -9, and -12 genes in relation to subarachnoid hemorrhageB Zhang, S Dhillon, I Geary, et al.
Journal of Lipid Research|June 5, 1999
Evidence for a third genetic locus causing familial hypercholesterolemia. A non-LDLR, non-APOB kindredL Haddad, I N Day, S Hunt, et al.
Clinical Genetics|July 11, 1998
Applicability of LDLR flanking microsatellite polymorphisms for prenatal diagnosis of homozygous state for familial hypercholesterolemiaE R De Oliveira e Silva, L Haddad, P O Kwiterovich, et al.
Journal of Medical Genetics|February 1, 1997
Identification of a common low density lipoprotein receptor mutation (R329X) in the south of England: complete linkage disequilibrium with an allele of microsatellite D19S394I N Day, L Haddad, S D O'Dell, et al.
Annals of Human Genetics|October 1, 1991
The gene for human neurone specific ubiquitin C-terminal hydrolase (UCHL1, PGP9.5) maps to chromosome 4p14Y H Edwards, M F Fox, S Povey, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|May 13, 1998
W64R mutation in beta-3-adrenergic receptor gene and weight in a large population sampleS D O'Dell, M K Bolla, G J Miller, et al.
Thrombosis and Haemostasis|December 22, 1999
Gene-environment interaction in the determination of levels of plasma fibrinogenS E Humphries, L A Luong, H E Montgomery, et al.
Human Mutation|January 1, 1997
Spectrum of LDL receptor gene mutations in heterozygous familial hypercholesterolemiaI N Day, R A Whittall, S D O'Dell, et al.
Human Mutation|January 1, 1997
A high incidence of mutations in exon 6 of the low-density lipoprotein receptor gene in Greek familial hypercholesterolemia patients, including a novel mutationN Mavroidis, J Traeger-Synodinos, E Kanavakis, et al.
Human Genetics|April 17, 1998
Analysis of low density lipoprotein receptor gene mutations and microsatellite haplotypes in Greek FH heterozygous children: six independent ancestors account for 60% of probandsJ Traeger-Synodinos, N Mavroidis, E Kanavakis, et al.
Pageof 8