[Modern aspects of the genetics of mental retardation]

[Thermodynamic functions of lysozyme, myoglobin, beta-lactoglobulin, albumin, and poly-L-tryptophane in the temperature range 0-330 K].

Biofizika·2001

[Identification of mutations in the arylsulfatase B gene in Russian mucopolysaccharidosis type VI patients].

Genetika·2000

[Information and retrieval diagnostic system for inherited metabolic diseases].

Vestnik Rossiiskoi akademii meditsinskikh nauk·2000

[Program for diagnosis and prevention of inherited metabolic diseases of cellular organelles].

Vestnik Rossiiskoi akademii meditsinskikh nauk·2000

[Monogenic hereditary diseases in Gorno-Mariĭskiĭ district of Mariĭ El republic].

Genetika·1996

[The first experience in Russia of using DNA diagnosis in Alport's syndrome in a family with a unique morphological picture of the kidney lesion].

Terapevticheskii arkhiv·1995

[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

Association of solute carrier family 19 member 1 (SLC19A1) A80G polymorphism with the maternal risk for having a child with Down syndrome: A systematic review and meta-analysis.

Mutation research. Reviews in mutation research·2026

Lethal Transaldolase Deficiency Mimicking Gestational Alloimmune Liver Disease: Prenatal Sonography and Identification of a Novel TALDO1 Variant.

AJP reports·2026

First report of the complete mitochondrial genome of Microtendipes famiefeus Sasa, 1996 (Diptera: Chironomidae).

Mitochondrial DNA. Part B, Resources·2026

Genetic origin and forensic analysis of han populations from four districts in Shanghai, China, based on Y-chromosome STR and SNP markers.

International journal of legal medicine·2026

A novel Doppler ultrasound approach for phenotypic assessment and follow-up of Klippel-Trénaunay syndrome: A retrospective multicenter study.

Phlebology·2026

A familial 22.59 Mb deletion of the 10q11.21q21.3 region on the neocentromeric chromosome 10 with coexistence of SMC(10): Case report and review of literature.

Cytogenetic and genome research·2026

Related Experiment Videos

[Modern aspects of the genetics of mental retardation]

Related Concept Videos

[Thermodynamic functions of lysozyme, myoglobin, beta-lactoglobulin, albumin, and poly-L-tryptophane in the temperature range 0-330 K].

[Identification of mutations in the arylsulfatase B gene in Russian mucopolysaccharidosis type VI patients].

[Information and retrieval diagnostic system for inherited metabolic diseases].

[Program for diagnosis and prevention of inherited metabolic diseases of cellular organelles].

[Monogenic hereditary diseases in Gorno-Mariĭskiĭ district of Mariĭ El republic].

[The first experience in Russia of using DNA diagnosis in Alport's syndrome in a family with a unique morphological picture of the kidney lesion].

[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].

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

[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].

Association of solute carrier family 19 member 1 (SLC19A1) A80G polymorphism with the maternal risk for having a child with Down syndrome: A systematic review and meta-analysis.

Lethal Transaldolase Deficiency Mimicking Gestational Alloimmune Liver Disease: Prenatal Sonography and Identification of a Novel TALDO1 Variant.

First report of the complete mitochondrial genome of Microtendipes famiefeus Sasa, 1996 (Diptera: Chironomidae).

Genetic origin and forensic analysis of han populations from four districts in Shanghai, China, based on Y-chromosome STR and SNP markers.

A novel Doppler ultrasound approach for phenotypic assessment and follow-up of Klippel-Trénaunay syndrome: A retrospective multicenter study.

A familial 22.59 Mb deletion of the 10q11.21q21.3 region on the neocentromeric chromosome 10 with coexistence of SMC(10): Case report and review of literature.

Related Experiment Videos

[Modern aspects of the genetics of mental retardation]

Related Concept Videos

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