To the 100th anniversary of Vladimir Pavlovich Efroimson (1908–1989) E. A. Keshman Announcement 16 October 2008 Pages: 1127 - 1133
Monogenic hypercholesterolemias: New genes, new drug targets M. Y. MandelshtamV. B. Vasilyev Reviews and Theoretical Articles 16 October 2008 Pages: 1134 - 1140
Hereditary diseases among Yakuts V. P. PuzyrevN. P. Maximova Reviews and Theoretical Articles 16 October 2008 Pages: 1141 - 1147
Molecular genetic basis of proximal spinal muscular atrophy and experience in its pharmaceutical treatment V. S. BaranovA. V. KiselevA. N. Baranov Reviews and Theoretical Articles 16 October 2008 Pages: 1148 - 1159
Adipokine genetics: Unbalanced protein secretion by human adipose tissue as a cause of the metabolic syndrome A. V. Baranova Reviews and Theoretical Articles 16 October 2008 Pages: 1160 - 1175
Epimutations of imprinted genes in the human genome: Classification, causes, association with hereditary pathology I. N. LebedevE. A. Sazhenova Reviews and Theoretical Articles 16 October 2008 Pages: 1176 - 1190
The spectrum of mutations in the low-density lipoprotein receptor gene in the Russian population M. I. VoevodaI. V. KulikovYu. P. Nikitin Experimental Articles 16 October 2008 Pages: 1191 - 1194
From clinical and biochemical to molecular genetic diagnosis of Wilson disease in Latvia A. KruminaJ. KeissB. Rozentale Experimental Articles 16 October 2008 Pages: 1195 - 1200
Spectrum and frequency of mutations in the connexin 32 gene (GJB1) in hereditary and sensory neuropathy type 1X patients from Bashkortostan I. M. KhidiyatovaE. G. BagautdinovaE. K. Khusnutdinova Experimental Articles 16 October 2008 Pages: 1201 - 1207
TGFBI gene mutations in the Ukrainian patients with inherited corneal stromal dystrophies V. N. PampukhaS. A. KravchenkoL. A. Livshits Experimental Articles 16 October 2008 Pages: 1208 - 1211
Predicting a clinical/biochemical phenotype for PKU/MHP patients with PAH gene mutations J. KasnauskienėL. CimbalistienėV. Kučinskas Experimental Articles 16 October 2008 Pages: 1212 - 1218
Molecular genetic characteristics of Duchenne-Becker muscular dystrophy in the Republic of Moldova V. Sacare Experimental Articles 16 October 2008 Pages: 1219 - 1223
Genetic diversity and the structure of linkage disequilibrium in the methylenetetrahydrofolate reductase locus E. A. TrifonovaM. G. SpiridonovaV. A. Stepanov Experimental Articles 16 October 2008 Pages: 1224 - 1232
Mutational spectrum of the gene for 21-hydroxylase in the patients with congenital adrenal hyperplasia from Bashkortostan V. L. AkhmetovaZ. F. RamovaE. K. Khusnutdinova Experimental Articles 16 October 2008 Pages: 1233 - 1240
Glutathione-S-transferase gene polymorphism in Russian populations of European part of Russia A. V. KhruninD. V. KhokhrinS. A. Limborska Experimental Articles 16 October 2008 Pages: 1241 - 1245
Independent origin of rare Y168H mutation of human phenylalanine hydroxylase gene in Russia E. V. BrennerF. O. SmagulovaI. V. Morozov Brief Communications 16 October 2008 Pages: 1246 - 1248
“Molecular Analysis of Some Genes from Plasmid p19 of the Bacillus subtilis 19 Soil Strain Involved in Conjugation” E. U. PoluektovaE. Yu. GagarinaA. A. Prozorov Erratum 16 October 2008 Pages: 1249 - 1249