[Intrauterine diagnosis of G-G translocation]

Plasma carnitine ester profile in homozygous and heterozygous OCTN2 deficiency.

Journal of inherited metabolic disease·2009

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

Acta biologica Hungarica·2006

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

American journal of medical genetics·2002

Increased frequency of the C3*F allele and the Leiden mutation of coagulation factor V in patients with severe coronary heart disease who survived myocardial infarction.

Experimental and clinical immunogenetics·2002

[Centromere separation and malignancy].

Orvosi hetilap·2000

No evidence of uniparental disomy 2, 6, 14, 16, 20, and 22 as a major cause of intrauterine growth retardation.

Clinical genetics·2000

[What is (not) considered normal? - Contemporary challenges of establishing laboratory reference intervals].

Orvosi hetilap·2026

[Barriers to the timely initiation of hospice-palliative care in the Hungarian healthcare system].

Orvosi hetilap·2026

[A retrospective study of dental care under general anesthesia for children with special needs].

Orvosi hetilap·2026

[Chest wall reconstruction with biological mesh].

Orvosi hetilap·2026

[Structured data collection during neonatal anesthesia: Neo Somno Log - a self-developed digital event tracker].

Orvosi hetilap·2026

[Assessment of dietary habits in adolescents with inflammatory bowel disease].

Orvosi hetilap·2026

A Novel Technique for Validating Copy Number Variants and Its Application in Familial Exudative Vitreoretinopathy.

Human mutation·2026

The genome sequence of Gardnerycteris keenani (Chiroptera, Phyllostomidae, Stenodermatinae; Handley, 1960).

Wellcome open research·2026

The genome sequence of Filago lutescens Jord., 1846 (Asterales: Asteraceae).

Wellcome open research·2026

Common genetic variants are associated with increased likelihood of latent co-occurring neurodevelopmental and mental health factors among autistic individuals.

Molecular psychiatry·2026

Associations between brain phenotypes and temporomandibular disorders: An integrative multi-omics investigation.

Cranio : the journal of craniomandibular practice·2026

Bidirectional Regulation of Stress Responses by the Microbiota-Gut-Brain Axis: Molecular Mechanisms and Therapeutic Perspectives.

Physiology & behavior·2026

Related Experiment Videos

[Intrauterine diagnosis of G-G translocation]

Related Concept Videos

Plasma carnitine ester profile in homozygous and heterozygous OCTN2 deficiency.

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

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

Increased frequency of the C3*F allele and the Leiden mutation of coagulation factor V in patients with severe coronary heart disease who survived myocardial infarction.

[Centromere separation and malignancy].

No evidence of uniparental disomy 2, 6, 14, 16, 20, and 22 as a major cause of intrauterine growth retardation.

[What is (not) considered normal? - Contemporary challenges of establishing laboratory reference intervals].

[Barriers to the timely initiation of hospice-palliative care in the Hungarian healthcare system].

[A retrospective study of dental care under general anesthesia for children with special needs].

[Chest wall reconstruction with biological mesh].

[Structured data collection during neonatal anesthesia: Neo Somno Log - a self-developed digital event tracker].

[Assessment of dietary habits in adolescents with inflammatory bowel disease].

A Novel Technique for Validating Copy Number Variants and Its Application in Familial Exudative Vitreoretinopathy.

The genome sequence of Gardnerycteris keenani (Chiroptera, Phyllostomidae, Stenodermatinae; Handley, 1960).

The genome sequence of Filago lutescens Jord., 1846 (Asterales: Asteraceae).

Common genetic variants are associated with increased likelihood of latent co-occurring neurodevelopmental and mental health factors among autistic individuals.

Associations between brain phenotypes and temporomandibular disorders: An integrative multi-omics investigation.

Bidirectional Regulation of Stress Responses by the Microbiota-Gut-Brain Axis: Molecular Mechanisms and Therapeutic Perspectives.

Related Experiment Videos

[Intrauterine diagnosis of G-G translocation]

Related Concept Videos

Related Articles