Add to ORKGGeisel J, Oette K, Weisshaar B. Diagnosis of Familial Hypercholesterolemia using DNA probes for the Low-density Lipoprotein Receptor gene. In: Henke J, Kömpf J, Driesel AJ, eds. DNA-Polymorphism in Forensic and Medicine. BioTechForum. Vol 1. Heidelberg: Hüthig; 1990: 31-46
The aim of our study was to define mutations causing familial hypercholesterolemia (FH) phenotype in...
Familial hypercholesterolaemia is a common inherited disorder characterized by abnormally elevated s...
Objective: Familial Hypercholesterolemia (FH) is a metabolic disorder inherited as an autosomal domi...
Cardiovascular disease is the leading cause of death worldwide and, like most chronic diseases, it h...
Abstract Background and objectives: Familial hypercholesterolemia (FH) is an autosomal disorder char...
AIMS: We assembled a cohort of patients with familial hypercholesterolaemia (FH) for both basic and ...
High specificity makes DNA screening the method of choice for diagnosis of familial hypercholesterol...
Aims We assembled a cohort of patients with familial hypercholesterolaemia (FH) for both basic and c...
AIMS: We assembled a cohort of patients with familial hypercholesterolaemia (FH) for both basic and ...
Familial hypercholesterolemia (FH) manifested as atherosclerosis is a major cause of coronary heart ...
Familial Hypercholesterolaemia (FH) is one of the most common monogenic disorders, being caused most...
Aim: Familial hypercholesterolaemia (FH) is an autosomal dominant disorder that confers an increased...
Objectives: The aim of this study was to combine clinical criteria and next-generation sequencing (p...
Prenatal diagnosis for familial hypercholesterolaemia (FH) was performed by using restriction fragme...
The diagnosis of familial hypercholesterolemia (FH) in unselected children is difficult due to the f...
The aim of our study was to define mutations causing familial hypercholesterolemia (FH) phenotype in...
Familial hypercholesterolaemia is a common inherited disorder characterized by abnormally elevated s...
Objective: Familial Hypercholesterolemia (FH) is a metabolic disorder inherited as an autosomal domi...
Cardiovascular disease is the leading cause of death worldwide and, like most chronic diseases, it h...
Abstract Background and objectives: Familial hypercholesterolemia (FH) is an autosomal disorder char...
AIMS: We assembled a cohort of patients with familial hypercholesterolaemia (FH) for both basic and ...
High specificity makes DNA screening the method of choice for diagnosis of familial hypercholesterol...
Aims We assembled a cohort of patients with familial hypercholesterolaemia (FH) for both basic and c...
AIMS: We assembled a cohort of patients with familial hypercholesterolaemia (FH) for both basic and ...
Familial hypercholesterolemia (FH) manifested as atherosclerosis is a major cause of coronary heart ...
Familial Hypercholesterolaemia (FH) is one of the most common monogenic disorders, being caused most...
Aim: Familial hypercholesterolaemia (FH) is an autosomal dominant disorder that confers an increased...
Objectives: The aim of this study was to combine clinical criteria and next-generation sequencing (p...
Prenatal diagnosis for familial hypercholesterolaemia (FH) was performed by using restriction fragme...
The diagnosis of familial hypercholesterolemia (FH) in unselected children is difficult due to the f...
The aim of our study was to define mutations causing familial hypercholesterolemia (FH) phenotype in...
Familial hypercholesterolaemia is a common inherited disorder characterized by abnormally elevated s...
Objective: Familial Hypercholesterolemia (FH) is a metabolic disorder inherited as an autosomal domi...