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The Genome Structure and DNA Diagnosis of Monogenic Hereditary Disorders in the Volga–Ural Region.
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- Molecular Biology, 2004, v. 38, n. 1, p. 119, doi. 10.1023/B:MBIL.0000015147.20967.7d
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- Article
Analysis of Polymorphisms of the Huntington Disease Gene in Ethnic Populations of the Volga–Ural Region.
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- Molecular Biology, 2003, v. 37, n. 6, p. 818, doi. 10.1023/B:MBIL.0000008348.94676.e0
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- Article
Frequency of the 35delG Mutation of the Connexin 26 Gene (GJB2) in Patients with Non-Syndromic Recessive Deafness from Bashkortostan and in Ethnic Groups of the Volga–Ural Region.
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- Molecular Biology, 2002, v. 36, n. 3, p. 338, doi. 10.1023/A:1016047010528
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Study of the Role of Genes Involved in the Metabolism of Histamine in the Development of Allergic Respiratory Diseases.
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- Russian Journal of Genetics, 2024, v. 60, n. 3, p. 352, doi. 10.1134/S1022795424030128
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Analysis of ATL1 Gene Mutations and Clinical Features of the Disease Course in Patients with Hereditary Spastic Paraplegia.
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- Russian Journal of Genetics, 2022, v. 58, n. 9, p. 1145, doi. 10.1134/S1022795422090113
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- Article
Major Mutation in the SPAST Gene in Patients with Autosomal Dominant Spastic Paraplegia from the Republic of Bashkortostan.
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- Russian Journal of Genetics, 2019, v. 55, n. 2, p. 259, doi. 10.1134/S1022795419020091
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- Article
Two novel mutations in gene SPG4 in patients with autosomal dominant spastic paraplegia.
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- Russian Journal of Genetics, 2016, v. 52, n. 6, p. 603, doi. 10.1134/S1022795416060028
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- Article
Role of allelic genes of matrix metalloproteinases and their tissue inhibitors in the risk of peptic ulcer disease development.
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- Russian Journal of Genetics, 2016, v. 52, n. 3, p. 320, doi. 10.1134/S1022795416020113
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- Article
Association of cytokine gene polymorphisms in peptic ulcer development in the Bashkortostan Republic.
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- Russian Journal of Genetics, 2014, v. 50, n. 12, p. 1316, doi. 10.1134/S1022795414120084
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MFN2 gene analysis in patients with hereditary motor and sensory neuropathy from Bashkortostan Republic.
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- Russian Journal of Genetics, 2013, v. 49, n. 7, p. 771, doi. 10.1134/S1022795413060045
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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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Spectrum and frequency of mutations in the connexin 32 gene ( GJB1) in hereditary and sensory neuropathy type 1X patients from Bashkortostan.
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- Russian Journal of Genetics, 2008, v. 44, n. 10, p. 1201, doi. 10.1134/S1022795408100098
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- Article
Analysis of the IT15 Gene in Huntington's Disease Families.
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- Russian Journal of Genetics, 2004, v. 40, n. 8, p. 919, doi. 10.1023/B:RUGE.0000039726.96053.78
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- Article
Distribution of the HLA-DRB1 Specificities in Populations of the Volga–Ural Region.
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- Russian Journal of Genetics, 2004, v. 40, n. 2, p. 203, doi. 10.1023/B:RUGE.0000016996.85196.49
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- Article
Analysis of Deletion Mutations in the PARK2 Gene in Idiopathic Parkinson's Disease.
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- Russian Journal of Genetics, 2003, v. 39, n. 2, p. 166, doi. 10.1023/A:1022427708736
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- Article
Depression and Anxiety in Parkinson’s Disease.
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- Neuroscience & Behavioral Physiology, 2018, v. 48, n. 5, p. 636, doi. 10.1007/s11055-018-0609-1
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- Article