Hereditary diseases among Yakuts.
- Published in:
- Russian Journal of Genetics, 2008, v. 44, n. 10, p. 1141, doi. 10.1134/S1022795408100037
- By:
- Publication type:
- Article
Works matching IS 10227954 AND DT 2008 AND VI 44 AND IP 10
Results: 17
1
2
Genetic diversity and the structure of linkage disequilibrium in the methylenetetrahydrofolate reductase locus.
- Published in:
- Russian Journal of Genetics, 2008, v. 44, n. 10, p. 1224, doi. 10.1134/S102279540810013X
- By:
- Publication type:
- Article
3
From clinical and biochemical to molecular genetic diagnosis of Wilson disease in Latvia.
- Published in:
- Russian Journal of Genetics, 2008, v. 44, n. 10, p. 1195, doi. 10.1134/S1022795408100086
- By:
- Publication type:
- Article
4
Spectrum and frequency of mutations in the connexin 32 gene ( GJB1) in hereditary and sensory neuropathy type 1X patients from Bashkortostan.
- Published in:
- Russian Journal of Genetics, 2008, v. 44, n. 10, p. 1201, doi. 10.1134/S1022795408100098
- By:
- Publication type:
- Article
5
TGFBI gene mutations in the Ukrainian patients with inherited corneal stromal dystrophies.
- Published in:
- Russian Journal of Genetics, 2008, v. 44, n. 10, p. 1208, doi. 10.1134/S1022795408100104
- By:
- Publication type:
- Article
6
Predicting a clinical/biochemical phenotype for PKU/MHP patients with PAH gene mutations.
- Published in:
- Russian Journal of Genetics, 2008, v. 44, n. 10, p. 1212, doi. 10.1134/S1022795408100116
- By:
- Publication type:
- Article
7
Molecular genetic characteristics of Duchenne-Becker muscular dystrophy in the Republic of Moldova.
- Published in:
- Russian Journal of Genetics, 2008, v. 44, n. 10, p. 1219, doi. 10.1134/S1022795408100128
- By:
- Publication type:
- Article
8
Mutational spectrum of the gene for 21-hydroxylase in the patients with congenital adrenal hyperplasia from Bashkortostan.
- Published in:
- Russian Journal of Genetics, 2008, v. 44, n. 10, p. 1233, doi. 10.1134/S1022795408100141
- By:
- Publication type:
- Article
9
Glutathione-S-transferase gene polymorphism in Russian populations of European part of Russia.
- Published in:
- Russian Journal of Genetics, 2008, v. 44, n. 10, p. 1241, doi. 10.1134/S1022795408100153
- By:
- Publication type:
- Article
10
Independent origin of rare Y168H mutation of human phenylalanine hydroxylase gene in Russia.
- Published in:
- Russian Journal of Genetics, 2008, v. 44, n. 10, p. 1246, doi. 10.1134/S1022795408100165
- By:
- Publication type:
- Article
11
“Molecular Analysis of Some Genes from Plasmid p19 of the Bacillus subtilis 19 Soil Strain Involved in Conjugation”.
- Published in:
- 2008
- By:
- Publication type:
- Correction Notice
12
The spectrum of mutations in the low-density lipoprotein receptor gene in the Russian population.
- Published in:
- Russian Journal of Genetics, 2008, v. 44, n. 10, p. 1191, doi. 10.1134/S1022795408100074
- By:
- Publication type:
- Article
13
To the 100<sup>th</sup> anniversary of Vladimir Pavlovich Efroimson (1908–1989).
- Published in:
- 2008
- By:
- Publication type:
- Obituary
14
Monogenic hypercholesterolemias: New genes, new drug targets.
- Published in:
- Russian Journal of Genetics, 2008, v. 44, n. 10, p. 1134, doi. 10.1134/S1022795408100025
- By:
- Publication type:
- Article
15
Molecular genetic basis of proximal spinal muscular atrophy and experience in its pharmaceutical treatment.
- Published in:
- Russian Journal of Genetics, 2008, v. 44, n. 10, p. 1148, doi. 10.1134/S1022795408100049
- By:
- Publication type:
- Article
16
Adipokine genetics: Unbalanced protein secretion by human adipose tissue as a cause of the metabolic syndrome.
- Published in:
- Russian Journal of Genetics, 2008, v. 44, n. 10, p. 1160, doi. 10.1134/S1022795408100050
- By:
- Publication type:
- Article
17
Epimutations of imprinted genes in the human genome: Classification, causes, association with hereditary pathology.
- Published in:
- Russian Journal of Genetics, 2008, v. 44, n. 10, p. 1176, doi. 10.1134/S1022795408100062
- By:
- Publication type:
- Article