Add to ORKGsequencing of afilnity-captured amplified human DNA: application to the detection of apolipoprotein E polymorphisms. FEBS Let
Familial Hypercholesterolemia (FH) results in elevated levels of blood lipids including total choles...
Objective: Familial Hypercholesterolemia (FH) is a metabolic disorder inherited as an autosomal domi...
Low-density lipoprotein (LDL) size, a coronary heart disease risk factor, is influenced by both gene...
Familial hypercholesterolemia (FH) has an estimated frequency of 1:154 among French Canadians in Nor...
Familial hypercholesterolemia (FH) is one of the most common autosomal codominant diseases. FH is ca...
AbstractA cDNA probe for the low density lipoprotein (LDL) receptor gene was used to screen DNA samp...
To investigate the molecular basis of familial hypercholesterolemia (FH) in France, we applied the s...
The aim of this study was to detect mutations in the genes coding for the low-density lipoprotein re...
Familial hypercholesterolemia (FH) is a metabolic disorder inherited as an autosomal dominant trait ...
From a large cohort of hyperlipidemic patients, who attended the Lipid Research Clinic in Amsterdam,...
The aim of our study was to define mutations causing familial hypercholesterolemia (FH) phenotype in...
A total of 35 homozygous and 1320 heterozygous patients with familial hypercholesterolemia (FH) was ...
Geisel J, Oette K, Weisshaar B. Diagnosis of Familial Hypercholesterolemia using DNA probes for the ...
Familial hypercholesterolemia (FH) is a genetic condition characterized by a high cholesterol concen...
Autosomal dominant hypercholesterolemia (ADH) is a human disorder characterized phenotypically by is...
Familial Hypercholesterolemia (FH) results in elevated levels of blood lipids including total choles...
Objective: Familial Hypercholesterolemia (FH) is a metabolic disorder inherited as an autosomal domi...
Low-density lipoprotein (LDL) size, a coronary heart disease risk factor, is influenced by both gene...
Familial hypercholesterolemia (FH) has an estimated frequency of 1:154 among French Canadians in Nor...
Familial hypercholesterolemia (FH) is one of the most common autosomal codominant diseases. FH is ca...
AbstractA cDNA probe for the low density lipoprotein (LDL) receptor gene was used to screen DNA samp...
To investigate the molecular basis of familial hypercholesterolemia (FH) in France, we applied the s...
The aim of this study was to detect mutations in the genes coding for the low-density lipoprotein re...
Familial hypercholesterolemia (FH) is a metabolic disorder inherited as an autosomal dominant trait ...
From a large cohort of hyperlipidemic patients, who attended the Lipid Research Clinic in Amsterdam,...
The aim of our study was to define mutations causing familial hypercholesterolemia (FH) phenotype in...
A total of 35 homozygous and 1320 heterozygous patients with familial hypercholesterolemia (FH) was ...
Geisel J, Oette K, Weisshaar B. Diagnosis of Familial Hypercholesterolemia using DNA probes for the ...
Familial hypercholesterolemia (FH) is a genetic condition characterized by a high cholesterol concen...
Autosomal dominant hypercholesterolemia (ADH) is a human disorder characterized phenotypically by is...
Familial Hypercholesterolemia (FH) results in elevated levels of blood lipids including total choles...
Objective: Familial Hypercholesterolemia (FH) is a metabolic disorder inherited as an autosomal domi...
Low-density lipoprotein (LDL) size, a coronary heart disease risk factor, is influenced by both gene...