[Current tastks of genetic counseling centers]

Mutations of the apolipoprotein A5 gene with inherited hypertriglyceridaemia: review of the current literature.

Current medicinal chemistry·2012

Mosaic supernumerary ring chromosome 1 in a three-generational family: 10-year follow-up report.

European journal of medical genetics·2010

Excess of malignancies in grandparents of children with malformations? Short communication.

Acta biologica Hungarica·2006

Increased prevalence of factor V Leiden mutation in premature but not in full-term infants with grade I intracranial haemorrhage.

Biology of the neonate·2004

Mitochondrial DNA4977 deletion in brain of newborns died after intensive care.

Acta biologica Hungarica·2004

Association of nonsyndromic Wilms tumor with premature centromere division (PCD).

American journal of medical genetics·2002

[A burning challenge in emergency care: burnout, secondary traumatic stress, and psychological immune competence].

Orvosi hetilap·2026

[Triptan treatment in migraine: a dose-based model for persistence and acute medication use patterns using nationwide health insurance data].

Orvosi hetilap·2026

[Patient satisfaction and complications following penile prosthesis implantation].

Orvosi hetilap·2026

[Introducing triage-initiated imaging examinations at a Hungarian emergency department].

Orvosi hetilap·2026

[Tumour-like extramedullary hematopoiesis in a patient with multiple renal transplantations].

Orvosi hetilap·2026

[A review of the European Resuscitation Council (ERC) 2025 first aid and adult basic life support practical guidelines: implications for Hungarian practice].

Orvosi hetilap·2026

Wilson disease associated with a novel variant in the ATP7B gene.

Frontiers in neurology·2026

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Scientific reports·2026

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Journal of genetics and genomics = Yi chuan xue bao·2026

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Clinica chimica acta; international journal of clinical chemistry·2026

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

Brain & development·2026

High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.

The Journal of heredity·2026

Related Experiment Videos

[Current tastks of genetic counseling centers]

Related Concept Videos

Mutations of the apolipoprotein A5 gene with inherited hypertriglyceridaemia: review of the current literature.

Mosaic supernumerary ring chromosome 1 in a three-generational family: 10-year follow-up report.

Excess of malignancies in grandparents of children with malformations? Short communication.

Increased prevalence of factor V Leiden mutation in premature but not in full-term infants with grade I intracranial haemorrhage.

Mitochondrial DNA4977 deletion in brain of newborns died after intensive care.

Association of nonsyndromic Wilms tumor with premature centromere division (PCD).

[A burning challenge in emergency care: burnout, secondary traumatic stress, and psychological immune competence].

[Triptan treatment in migraine: a dose-based model for persistence and acute medication use patterns using nationwide health insurance data].

[Patient satisfaction and complications following penile prosthesis implantation].

[Introducing triage-initiated imaging examinations at a Hungarian emergency department].

[Tumour-like extramedullary hematopoiesis in a patient with multiple renal transplantations].

[A review of the European Resuscitation Council (ERC) 2025 first aid and adult basic life support practical guidelines: implications for Hungarian practice].

Wilson disease associated with a novel variant in the ATP7B gene.

Molecular characterization of FAM222B as a novel disease gene for dominant cardiovascular laterality defects.

Genetic architecture and inheritance patterns of Leber hereditary optic neuropathy among 419 Chinese pedigrees carrying the ND4 11778G>A mutation.

Integrating LNA-qPCR and full-length SMN1 sequencing for precision SMA carrier screening: large-scale validation in 30,849 individuals.

Novel splice site variants in GBA1 are associated with Gaucher disease and genotype-phenotype correlations.

High-Resolution Physical Mapping and Chromosomal Transmission in Sugarcane Progeny.

Related Experiment Videos

[Current tastks of genetic counseling centers]

Related Concept Videos

Related Articles