On the relationship between Lp(a) lipoprotein, "sinking pre-beta-lipoprotein" and inherited hyper-beta-lipoproteinaemia

Expanding the genotypic spectrum of Perrault syndrome.

Clinical genetics·2016

Familial adenomatous polyposis: mental health, psychosocial functioning and reactions to genetic risk in adolescents.

Clinical genetics·2010

Correlation between prenatal ultrasound and autopsy findings: A study of second-trimester abortions.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2006

The impact of an early truncating founder ATM mutation on immunoglobulins, specific antibodies and lymphocyte populations in ataxia-telangiectasia patients and their parents.

Clinical and experimental immunology·2004

[Genetic analysis in familial adenomatous polyposis].

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke·2002

[Need of better knowledge of genetic tests among Norwegian physicians].

Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke·2001

A New Case of Lethal Congenital Contracture Syndrome Type 3 With Hyperinsulinism and Optic Atrophy.

Clinical genetics·2026

Genetic Spectrum of Cholestasis in Tunisia and Diagnostic Yield of Next-Generation Sequencing: Case Series of 70 Patients.

Clinical genetics·2026

Childhood-Onset Filamin c Related Cardiomyopathy: Genotype-Phenotype Correlation and Outcome.

Clinical genetics·2026

A Homozygous Variant in DMRTB1 Is Associated With Non-Obstructive Azoospermia in Humans.

Clinical genetics·2026

Genetic Testing Unveils a Novel Thrombospondin-1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79-Year-Old Woman.

Clinical genetics·2026

A Novel De Novo STAG1 Variant at the RAD21 Binding Interface Is Associated With Hypoglycemia, Recurrent Fever, Immunodeficiency and Features of Classical Cohesinopathies.

Clinical genetics·2026

A gene-based pangenome reveals genomic divergence and altitudinal differentiation in allotetraploid quinoa.

Frontiers in plant science·2026

Evaluation of a Customized RDB-FTH Panel for β-Globin Variants in a Malaysian Tertiary Center.

Hemoglobin·2026

Coronal Subarachnoid-Space Measurements in Fetuses with Growth Restriction and Appropriate-for-Gestational-Age Controls: A Prospective Comparative Study.

Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine·2026

Longitudinal Clinical Progression in X-Linked Adrenoleukodystrophy: The AMNL Scoring System.

Annals of the Child Neurology Society·2026

Getting out of hand: niche construction theory and a multiplicity of handedness.

Laterality·2026

Accelerated biological ageing is associated with a large drusen burden.

Acta ophthalmologica·2026

Related Experiment Videos

On the relationship between Lp(a) lipoprotein, "sinking pre-beta-lipoprotein" and inherited

Related Concept Videos

Expanding the genotypic spectrum of Perrault syndrome.

Familial adenomatous polyposis: mental health, psychosocial functioning and reactions to genetic risk in adolescents.

Correlation between prenatal ultrasound and autopsy findings: A study of second-trimester abortions.

The impact of an early truncating founder ATM mutation on immunoglobulins, specific antibodies and lymphocyte populations in ataxia-telangiectasia patients and their parents.

[Genetic analysis in familial adenomatous polyposis].

[Need of better knowledge of genetic tests among Norwegian physicians].

A New Case of Lethal Congenital Contracture Syndrome Type 3 With Hyperinsulinism and Optic Atrophy.

Genetic Spectrum of Cholestasis in Tunisia and Diagnostic Yield of Next-Generation Sequencing: Case Series of 70 Patients.

Childhood-Onset Filamin c Related Cardiomyopathy: Genotype-Phenotype Correlation and Outcome.

A Homozygous Variant in DMRTB1 Is Associated With Non-Obstructive Azoospermia in Humans.

Genetic Testing Unveils a Novel Thrombospondin-1 Domain Containing Protein 1 Gene Variant as the Cause of Chronic Edema in a 79-Year-Old Woman.

A Novel De Novo STAG1 Variant at the RAD21 Binding Interface Is Associated With Hypoglycemia, Recurrent Fever, Immunodeficiency and Features of Classical Cohesinopathies.

A gene-based pangenome reveals genomic divergence and altitudinal differentiation in allotetraploid quinoa.

Evaluation of a Customized RDB-FTH Panel for β-Globin Variants in a Malaysian Tertiary Center.

Coronal Subarachnoid-Space Measurements in Fetuses with Growth Restriction and Appropriate-for-Gestational-Age Controls: A Prospective Comparative Study.

Longitudinal Clinical Progression in X-Linked Adrenoleukodystrophy: The AMNL Scoring System.

Getting out of hand: niche construction theory and a multiplicity of handedness.

Accelerated biological ageing is associated with a large drusen burden.

Related Experiment Videos

On the relationship between Lp(a) lipoprotein, "sinking pre-beta-lipoprotein" and inherited...

Related Concept Videos

Related Articles

On the relationship between Lp(a) lipoprotein, "sinking pre-beta-lipoprotein" and inherited