[Blood group markers in a Turkish family with sclerosing panencephalitis]

Initiation of H1-T6SS dueling between Pseudomonas aeruginosa.

mBio·2024

Transfluthrin Spatial Repellent on US Military Materials Reduces Culex tarsalis Incursion in a Desert Environment.

Journal of the American Mosquito Control Association·2020

Macroscopic phase separation of superconductivity and ferromagnetism in Sr0.5Ce0.5FBiS2-x Se x revealed by μSR.

Scientific reports·2017

A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1.

Leukemia·2016

Loss of function of PGAP1 as a cause of severe encephalopathy identified by Whole Exome Sequencing: Lessons of the bioinformatics pipeline.

Molecular and cellular probes·2015

Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.

JAMA·2015

[A screening method for rapid detection of barbiturates in serum using tandem mass spectrometry].

Beitrage zur gerichtlichen Medizin·1992

[Bolus death and drowning--expression of central nervous system dysregulation?].

Beitrage zur gerichtlichen Medizin·1992

[Toxic alcohol dysmyelopoiesis--bone marrow histology studies of a forensic medicine autopsy sample].

Beitrage zur gerichtlichen Medizin·1992

[Effect of ethanol on plasma amino acid concentration in man].

Beitrage zur gerichtlichen Medizin·1992

[Acute and chronic effect of alcohol--a long-term problem in forensic medicine autopsies].

Beitrage zur gerichtlichen Medizin·1992

[Alcohol drinking behavior in a sample of students].

Beitrage zur gerichtlichen Medizin·1992

Early-onset parkinsonism as a presenting feature of suspected type 1 Gaucher disease with two pathogenic GBA1 variants: a case report.

Frontiers in neuroscience·2026

Case Report: Proportionate short stature in a three-generation family harboring FGFR3 N540S: phenotypic expansion beyond hypochondroplasia and implications for genetic screening in idiopathic short stature.

Frontiers in endocrinology·2026

Proteogenomic analysis of pediatric and AYA high-grade glioma reveals age-dependent biology, female-male differences, and kinase targets.

Cell reports. Medicine·2026

ADNP-Related Helsmoortel-Van der Aa Syndrome: A Review of the Literature and Clinical Recommendations for Assessment and Monitoring.

American journal of medical genetics. Part A·2026

Parsing heterogeneity in autism spectrum disorder.

Science (New York, N.Y.)·2026

A Novel Pathogenic Frameshift Variant Associated With Holt-Oram Syndrome: A Case Report.

Case reports in genetics·2026

Related Experiment Videos

[Blood group markers in a Turkish family with sclerosing panencephalitis]

Related Concept Videos

Initiation of H1-T6SS dueling between Pseudomonas aeruginosa.

Transfluthrin Spatial Repellent on US Military Materials Reduces Culex tarsalis Incursion in a Desert Environment.

Macroscopic phase separation of superconductivity and ferromagnetism in Sr0.5Ce0.5FBiS2-x Se x revealed by μSR.

A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1.

Loss of function of PGAP1 as a cause of severe encephalopathy identified by Whole Exome Sequencing: Lessons of the bioinformatics pipeline.

Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer.

[A screening method for rapid detection of barbiturates in serum using tandem mass spectrometry].

[Bolus death and drowning--expression of central nervous system dysregulation?].

[Toxic alcohol dysmyelopoiesis--bone marrow histology studies of a forensic medicine autopsy sample].

[Effect of ethanol on plasma amino acid concentration in man].

[Acute and chronic effect of alcohol--a long-term problem in forensic medicine autopsies].

[Alcohol drinking behavior in a sample of students].

Early-onset parkinsonism as a presenting feature of suspected type 1 Gaucher disease with two pathogenic GBA1 variants: a case report.

Case Report: Proportionate short stature in a three-generation family harboring FGFR3 N540S: phenotypic expansion beyond hypochondroplasia and implications for genetic screening in idiopathic short stature.

Proteogenomic analysis of pediatric and AYA high-grade glioma reveals age-dependent biology, female-male differences, and kinase targets.

ADNP-Related Helsmoortel-Van der Aa Syndrome: A Review of the Literature and Clinical Recommendations for Assessment and Monitoring.

Parsing heterogeneity in autism spectrum disorder.

A Novel Pathogenic Frameshift Variant Associated With Holt-Oram Syndrome: A Case Report.

Related Experiment Videos

[Blood group markers in a Turkish family with sclerosing panencephalitis]

Related Concept Videos

Related Articles