Lipoproteins in LCAT-deficiency

Chromosomal microaberrations in patients with epilepsy, intellectual disability, and congenital anomalies.

Clinical genetics·2013

Lipoprotein(a): resurrected by genetics.

Journal of internal medicine·2012

Parental origin of de novo cytogenetically balanced reciprocal non-Robertsonian translocations.

Cytogenetic and genome research·2012

Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysis.

Clinical genetics·2010

Whole genome amplification from microdissected chromosomes.

Cytogenetic and genome research·2009

Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations.

Journal of medical genetics·2007

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Humangenetik·1975

Climate associated variations in the human serum albumin level.

Humangenetik·1975

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Humangenetik·1975

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Humangenetik·1975

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

Humangenetik·1975

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Humangenetik·1975

Hereditary Hyperferritinemia Cataract Syndrome Mimicking Iron Overload in a Pediatric Patient With Coexisting HFE H63D Homozygosity.

Case reports in pediatrics·2026

Peeling Back the Layers.

Journal of the American Academy of Child and Adolescent Psychiatry·2026

Late-onset autoimmune diabetes in 2 octogenarians: diagnostic misclassification and therapeutic heterogeneity.

JCEM case reports·2026

Global Prevalence of Obsessive-Compulsive and Related Disorders: A Systematic Review and Modeling Study.

The American journal of psychiatry·2026

Neuromyelitis optica spectrum disorder: a 5-year experience in a tertiary hospital in Northern Vietnam.

Multiple sclerosis and related disorders·2026

Extraconal Orbital Cavernous Venous Malformations: An Incidental Finding.

Annals of African medicine·2026

Related Experiment Videos

Lipoproteins in LCAT-deficiency

Related Concept Videos

Chromosomal microaberrations in patients with epilepsy, intellectual disability, and congenital anomalies.

Lipoprotein(a): resurrected by genetics.

Parental origin of de novo cytogenetically balanced reciprocal non-Robertsonian translocations.

Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysis.

Whole genome amplification from microdissected chromosomes.

Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations.

Cytological and cytogenetical studies on brain tumors. VI. No evidence for a translocation in 22-monosomic meningiomas.

Climate associated variations in the human serum albumin level.

A technique for in situ karyotyping of primary amniotic fluid cell cultures.

Sister chromatid exchanges and chromatid interchanges in bloom's syndrome.

Trisomy 9p due to paternal translocation, t(9;13) (q13;q12).

The Bf locus in the HLA region of chromosome 6: linkage and association studies.

Hereditary Hyperferritinemia Cataract Syndrome Mimicking Iron Overload in a Pediatric Patient With Coexisting HFE H63D Homozygosity.

Peeling Back the Layers.

Late-onset autoimmune diabetes in 2 octogenarians: diagnostic misclassification and therapeutic heterogeneity.

Global Prevalence of Obsessive-Compulsive and Related Disorders: A Systematic Review and Modeling Study.

Neuromyelitis optica spectrum disorder: a 5-year experience in a tertiary hospital in Northern Vietnam.

Extraconal Orbital Cavernous Venous Malformations: An Incidental Finding.

Related Experiment Videos

Lipoproteins in LCAT-deficiency

Related Concept Videos

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