| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Adipokine genetics: Unbalanced protein secretion by human adipose tissue as a cause of the metabolic syndrome
|
Baranova, A. V.
|
|
2008
|
44 |
10 |
p. 1160-1175
|
artikel
|
| 2 |
Epimutations of imprinted genes in the human genome: Classification, causes, association with hereditary pathology
|
Lebedev, I. N.
|
|
2008
|
44 |
10 |
p. 1176-1190
|
artikel
|
| 3 |
From clinical and biochemical to molecular genetic diagnosis of Wilson disease in Latvia
|
Krumina, A.
|
|
2008
|
44 |
10 |
p. 1195-1200
|
artikel
|
| 4 |
Glutathione-S-transferase gene polymorphism in Russian populations of European part of Russia
|
Khrunin, A. V.
|
|
2008
|
44 |
10 |
p. 1241-1245
|
artikel
|
| 5 |
Hereditary diseases among Yakuts
|
Puzyrev, V. P.
|
|
2008
|
44 |
10 |
p. 1141-1147
|
artikel
|
| 6 |
Independent origin of rare Y168H mutation of human phenylalanine hydroxylase gene in Russia
|
Brenner, E. V.
|
|
2008
|
44 |
10 |
p. 1246-1248
|
artikel
|
| 7 |
“Molecular Analysis of Some Genes from Plasmid p19 of the Bacillus subtilis 19 Soil Strain Involved in Conjugation”
|
Poluektova, E. U.
|
|
2008
|
44 |
10 |
p. 1249
|
artikel
|
| 8 |
Molecular genetic basis of proximal spinal muscular atrophy and experience in its pharmaceutical treatment
|
Baranov, V. S.
|
|
2008
|
44 |
10 |
p. 1148-1159
|
artikel
|
| 9 |
Molecular genetic characteristics of Duchenne-Becker muscular dystrophy in the Republic of Moldova
|
Sacare, V.
|
|
2008
|
44 |
10 |
p. 1219-1223
|
artikel
|
| 10 |
Monogenic hypercholesterolemias: New genes, new drug targets
|
Mandelshtam, M. Y.
|
|
2008
|
44 |
10 |
p. 1134-1140
|
artikel
|
| 11 |
Mutational spectrum of the gene for 21-hydroxylase in the patients with congenital adrenal hyperplasia from Bashkortostan
|
Akhmetova, V. L.
|
|
2008
|
44 |
10 |
p. 1233-1240
|
artikel
|
| 12 |
Predicting a clinical/biochemical phenotype for PKU/MHP patients with PAH gene mutations
|
Kasnauskienė, J.
|
|
2008
|
44 |
10 |
p. 1212-1218
|
artikel
|
| 13 |
Spectrum and frequency of mutations in the connexin 32 gene (GJB1) in hereditary and sensory neuropathy type 1X patients from Bashkortostan
|
Khidiyatova, I. M.
|
|
2008
|
44 |
10 |
p. 1201-1207
|
artikel
|
| 14 |
TGFBI gene mutations in the Ukrainian patients with inherited corneal stromal dystrophies
|
Pampukha, V. N.
|
|
2008
|
44 |
10 |
p. 1208-1211
|
artikel
|
| 15 |
The spectrum of mutations in the low-density lipoprotein receptor gene in the Russian population
|
Voevoda, M. I.
|
|
2008
|
44 |
10 |
p. 1191-1194
|
artikel
|
| 16 |
To the 100th anniversary of Vladimir Pavlovich Efroimson (1908–1989)
|
Keshman, E. A.
|
|
2008
|
44 |
10 |
p. 1127-1133
|
artikel
|
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