Found: 23
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Laminopathies in Russian families.
- Published in:
- Clinical Genetics, 2008, v. 74, n. 2, p. 127, doi. 10.1111/j.1399-0004.2008.01045.x
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- Article
Whole exome sequencing links dental tumor to an autosomal-dominant mutation in ANO5 gene associated with gnathodiaphyseal dysplasia and muscle dystrophies.
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- Scientific Reports, 2016, p. 26440, doi. 10.1038/srep26440
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- Article
Expression Profiles of Genes--Potential Therapy Targets--and Their Relationship to Survival in Renal Cell Carcinoma.
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- Doklady Biochemistry & Biophysics, 2018, v. 478, n. 1, p. 14, doi. 10.1134/S1607672918010040
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- Article
Spectrum of CFTR mutations in Chechen cystic fibrosis patients: high frequency of c.1545_1546delTA (p.Tyr515X; 1677delTA) and c.274G>A (p.Glu92Lys, E92K) mutations in North Caucasus.
- Published in:
- BMC Medical Genetics, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s12881-019-0785-z
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- Article
On the 70th Birthday of Vladimir Il'ich Ivanov.
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- Russian Journal of Developmental Biology, 2003, v. 34, n. 1, p. 57, doi. 10.1023/A:1022293902645
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- Article
Study of the Karachay Population Based on the Analysis of Ten Polymorphic DNA Loci.
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- Russian Journal of Genetics, 2024, v. 60, n. 2, p. 180, doi. 10.1134/S102279542402011X
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- Article
Diversity of Monogenic Hereditary Diseases in the Russian Population of the Volga-Ural Region.
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- Russian Journal of Genetics, 2021, v. 57, n. 11, p. 1356, doi. 10.1134/S1022795421110168
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- Article
Clinical Population Genetics of Hereditary Diseases among Children of the Karachay-Cherkess Republic.
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- Russian Journal of Genetics, 2019, v. 55, n. 8, p. 1033, doi. 10.1134/S1022795419080180
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- Article
Study of the Role of the Main Factors of Population Dynamics in the Mechanism of Differentiation and Formation of Diversity and Genetic Load of Hereditary Diseases in Subpopulations of the Karachay-Cherkess Republic.
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- Russian Journal of Genetics, 2019, v. 55, n. 6, p. 738, doi. 10.1134/S1022795419060206
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- Article
Russians of the Karachay-Cherkess Republic: Population Genetic Portrait.
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- Russian Journal of Genetics, 2018, v. 54, n. 9, p. 1117, doi. 10.1134/S1022795418090077
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- Article
Diversity and Prevalence of Hereditary Diseases among Nogais of the Karachay-Cherkess Republic.
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- Russian Journal of Genetics, 2018, v. 54, n. 7, p. 858, doi. 10.1134/S1022795418070165
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- Article
Medical Genetic Study of Hereditary Diseases in Abazins of the Karachay-Cherkess Republic.
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- Russian Journal of Genetics, 2018, v. 54, n. 6, p. 703, doi. 10.1134/S1022795418060170
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- Article
Genetic epidemiological study of Bashkortostan Republic: The effect of genetic structure of population on the load of monogenic hereditary diseases.
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- Russian Journal of Genetics, 2009, v. 45, n. 4, p. 478, doi. 10.1134/S1022795409040139
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- Article
Genetic structure of the Udmurt population.
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- Russian Journal of Genetics, 2007, v. 43, n. 8, p. 918, doi. 10.1134/S1022795407080145
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- Article
Population study of the Udmurt population: Analysis of ten polymorphic DNA loci of the nuclear genome.
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- Russian Journal of Genetics, 2007, v. 43, n. 5, p. 563, doi. 10.1134/S1022795407050122
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- Article
Integrated Population Genetic and Medical Genetic Study of Two Raions of the Tver Oblast.
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- Russian Journal of Genetics, 2004, v. 40, n. 5, p. 537
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- Article
Population-Genetic Structure of Chuvash Populations Inferred from the Data on Eight DNA Loci of the Nuclear Genome.
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- Russian Journal of Genetics, 2003, v. 39, n. 11, p. 1313, doi. 10.1023/B:RUGE.0000004147.09917.b7
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- Article
Yu. P. Altukhov, Genetic Processes in Populations, Moscow: Akademkniga, 2003.
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- 2003
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- Book Review
Prevalence and Molecular Genetic Typing of Nonsyndromic Sensorineural Deafness in Chuvash Republic.
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- Russian Journal of Genetics, 2003, v. 39, n. 9, p. 1076, doi. 10.1023/A:1025739521156
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- Article
Time Dynamics of Ethnic Assortativeness in Tsivil'sk Raion of Chuvashia.
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- Russian Journal of Genetics, 2003, v. 39, n. 4, p. 461, doi. 10.1023/A:1023374118250
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- Article
Genetic and Demographic Structure of Russian Populations from Tver and Rostov Oblast.
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- Russian Journal of Genetics, 2003, v. 39, n. 1, p. 91, doi. 10.1023/A:1022083113645
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- Article
Haemophilia: strategies for carrier detection and prenatal diagnosis.
- Published in:
- Bulletin of the World Health Organization, 1993, v. 71, n. 3/4, p. 429
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- Article
Complete screening of mutations in the coding sequence of the CFTR gene in a sample of CF patients from Russia: Identification of three novel alleles.
- Published in:
- Human Mutation, 1995, v. 5, n. 3, p. 205, doi. 10.1002/humu.1380050304
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- Article