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                             16 gevonden resultaten
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
                             16 gevonden resultaten
 
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