[Data on a population genetic study of hereditary systemic diseases of the skeleton]

[Improving renal cancer care].

Urologiia (Moscow, Russia : 1999)·2018

[The load and diversity of hereditary diseases in four raions of Rostov oblast].

Genetika·2015

A missense mutation of C1659 in the fibroblast growth factor receptor 3 gene in Russian patients with hypochondroplasia.

Endocrine journal·1999

[A medico-genetic description of inhabitants of two regions of the Kransnodar Krai].

Genetika·1999

[Molecular-genetic characteristics of the deleted region of chromosome 8q24.1 in Langer-Giedion and tricho-rhino-phalangeal type I syndromes].

Genetika·1996

[Genetic structure and the load of hereditary diseases in five populations of Arkhangel'skaia region].

Genetika·1996

[Radiologic consequences and medico-biological problems 4 years after the accident at the Chernobyl Atomic Electric Power Station].

Vestnik Akademii meditsinskikh nauk SSSR·1992

[Priority tasks of the common program for the clean-up of the consequences of the accident at the Chernobyl Atomic Electric Power Station].

Vestnik Akademii meditsinskikh nauk SSSR·1992

[Dynamics of the radiation conditions and evaluation of the radiation dosage of the inhabitants of Kiev following the accident at the Chernobyl Atomic Electric Power Station].

Vestnik Akademii meditsinskikh nauk SSSR·1992

[The relation of non-stochastic effects to the radiation dose of the human thyroid gland].

Vestnik Akademii meditsinskikh nauk SSSR·1992

[The significance of modifying factors in evaluating the effect of radionuclides].

Vestnik Akademii meditsinskikh nauk SSSR·1992

[Means of improving and characteristics of the use of beta spectrometry of 90Sr after the Chernobyl accident].

Vestnik Akademii meditsinskikh nauk SSSR·1992

Obesity and reduced renal corticomedullary differentiation on T1 mapping: a population-based UK Biobank study.

International urology and nephrology·2026

Evaluating the pathogenic significance of unique chromosomal variants in craniosynostosis using patient-derived induced pluripotent stem cells and mouse modelling.

Genetics in medicine : official journal of the American College of Medical Genetics·2026

[Genetic and functional characterization of a novel KIT splicing variant in a Chinese three-generation pedigree with piebaldism].

Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences·2026

Genome-wide association study of sarcopenia index reveals sex-stratified genetic architecture.

Biology of sex differences·2026

Whole-Exome Sequencing in a Consanguinity-Enriched South Indian Retinitis Pigmentosa Cohort: Diagnostic Yield and Molecular Spectrum.

Ophthalmology science·2026

Genetic analysis, reproductive decision-making, and pregnancy outcomes in 51 Chinese osteogenesis imperfecta families.

Journal of assisted reproduction and genetics·2026

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[Data on a population genetic study of hereditary systemic diseases of the skeleton]

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[Improving renal cancer care].

[The load and diversity of hereditary diseases in four raions of Rostov oblast].

A missense mutation of C1659 in the fibroblast growth factor receptor 3 gene in Russian patients with hypochondroplasia.

[A medico-genetic description of inhabitants of two regions of the Kransnodar Krai].

[Molecular-genetic characteristics of the deleted region of chromosome 8q24.1 in Langer-Giedion and tricho-rhino-phalangeal type I syndromes].

[Genetic structure and the load of hereditary diseases in five populations of Arkhangel'skaia region].

[Radiologic consequences and medico-biological problems 4 years after the accident at the Chernobyl Atomic Electric Power Station].

[Priority tasks of the common program for the clean-up of the consequences of the accident at the Chernobyl Atomic Electric Power Station].

[Dynamics of the radiation conditions and evaluation of the radiation dosage of the inhabitants of Kiev following the accident at the Chernobyl Atomic Electric Power Station].

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[The significance of modifying factors in evaluating the effect of radionuclides].

[Means of improving and characteristics of the use of beta spectrometry of 90Sr after the Chernobyl accident].

Obesity and reduced renal corticomedullary differentiation on T1 mapping: a population-based UK Biobank study.

Evaluating the pathogenic significance of unique chromosomal variants in craniosynostosis using patient-derived induced pluripotent stem cells and mouse modelling.

[Genetic and functional characterization of a novel KIT splicing variant in a Chinese three-generation pedigree with piebaldism].

Genome-wide association study of sarcopenia index reveals sex-stratified genetic architecture.

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