[Genetics and the future of man]

[Mutagenicity of drinking water in various districts of Moscow].

Genetika·1996

[Use of the micronucleus test for assessing the ecological situation in regions of the Astrakhan district].

Genetika·1994

Phenotypic and genetic affinities among ethnic populations in Daghestan (Caucasus, Russia): a comparison of polymorphic, physical, neurophysiological and psychological traits.

Annals of human biology·1993

[A.S. Serebrovskiĭ's experimental studies on induced mutagenesis].

Genetika·1992

[Rare variants of blood proteins in human populations].

Genetika·1988

[Heritability of neurodynamics and psychodynamics in human populations].

Genetika·1986

[Focal Neuropathies in SARS-CoV-2 Patients: Insights from a Single Center Experience].

Revista medica de Chile·2026

[Social Cognition and Theory of Mind as a Differential Marker Between Alzheimer's Disease and Behavioral Variant Frontotemporal Dementia].

Revista medica de Chile·2026

[Weight Recurrence After Bariatric Surgery: Definitions, Diagnosis, and Management Strategies. Part 2].

Revista medica de Chile·2026

[Perceptions of Communication Barriers Experienced by Migrants in Healthcare Services].

Revista medica de Chile·2026

[Gender Diversity and the Autism Spectrum: A Scoping Review of Experiences, Trajectories, and Emerging Needs Following the Cass Report].

Revista medica de Chile·2026

[Hepatic Overlap Syndrome: Primary Sclerosing Cholangitis and Primary Biliary Cholangitis. Case Review].

Revista medica de Chile·2026

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

Scientific reports·2026

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

The Lancet. Microbe·2026

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

Frontiers in genetics·2026

A Novel FN1 Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

Journal of clinical medicine·2026

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

HLA·2026

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Molecular syndromology·2026

Related Experiment Videos

[Genetics and the future of man]

Related Concept Videos

[Mutagenicity of drinking water in various districts of Moscow].

[Use of the micronucleus test for assessing the ecological situation in regions of the Astrakhan district].

Phenotypic and genetic affinities among ethnic populations in Daghestan (Caucasus, Russia): a comparison of polymorphic, physical, neurophysiological and psychological traits.

[A.S. Serebrovskiĭ's experimental studies on induced mutagenesis].

[Rare variants of blood proteins in human populations].

[Heritability of neurodynamics and psychodynamics in human populations].

[Focal Neuropathies in SARS-CoV-2 Patients: Insights from a Single Center Experience].

[Social Cognition and Theory of Mind as a Differential Marker Between Alzheimer's Disease and Behavioral Variant Frontotemporal Dementia].

[Weight Recurrence After Bariatric Surgery: Definitions, Diagnosis, and Management Strategies. Part 2].

[Perceptions of Communication Barriers Experienced by Migrants in Healthcare Services].

[Gender Diversity and the Autism Spectrum: A Scoping Review of Experiences, Trajectories, and Emerging Needs Following the Cass Report].

[Hepatic Overlap Syndrome: Primary Sclerosing Cholangitis and Primary Biliary Cholangitis. Case Review].

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

A Novel FN1 Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

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[Genetics and the future of man]

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