1. Tverskaya S., Dadali E., Evgrafov O. (1997) Prenatal DNA diagnosis in case of any monigenic hereditary disease with localized gene: a possible concept for DNA service. ESHG conference, abstract, Medizinische Genetik 9(2): 61
2. Baranov V., Zelenin A., Tarasenko O., Kolesnikov V., Mikhailov V., Ivaschenko T., Kiselev A., Evgrafov O., Dickson G., Shafei R., Artemyeva O., Kascheeva T., Baranov A. (1997) Human dystrophin gene expression in skeletal muscles of mdx mice after ballistic transfection. ESHG conference, abstract, Medizinische Genetik 9(2): 135.
3. Vasserman N., Tverskaya S., Karzakova L., Evgrafov O. (1997) Exclusion of linkage between autosomal recessive erythrocytosis and erythropoietin receptor gene. ESHG conference, abstract, Medizinische Genetik 9(2): 121.
4. Shagina I., Dadli E., Evgrafov O. (1997) SMN is the most probable candidate gene for recessive Starke-Kaeser scapuloperoneal spinal atrophy. ESHG conference, abstract, Medizinische Genetik 9(2): 131.
5. Chuhrova A., Vasserman N., Evgrafov O. (1997) A multiplex SSCP system for detection of dystrophin gene mutations and polymorphisms. ESHG conference, abstract, Medizinische Genetik 9(2): 148-149.
6. Mersiyanova I., Dadali E., Evgrafov O. (1997) Mutation analysis in patients with clinical diagnosis of Charcot-Marie-Tooth type 1. ESHG conference, abstract, Medizinische Genetik 9(2): 161.
7. Polyakov A., Tverskaya S., Osipova G., Dzenis I., Baharev V., Evgrafov O. (1997) Molecular study of 21-hydroxylase gene in groups of patients with polycystic ovary and Turner syndromes. ESHG conference, abstract, Medizinische Genetik 9(2): 166.
8. Zerjal T., Dashnyam B., Pandya A., Kayser M., Roewer L., Santos F.R., Schiefenhovel W., Fretwell N., Jobling M.A., Harihara S., Shimizu K., Semjidmaa D., Sajantila A., Salo P., Crawford M.H., Ginter E.K., Evgrafov O.V. and Tyler-Smith C. (1997) Genetic relationships of Asians and Northern Europeans, revealed by Y-chromosomal DNA analysis. Am. J. Hum. Genet. 60, 5, 1174-1183.
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9. Петрухин А.С., Заваденко Н.Н., Петрухин А.А., Евграфов О.В. (1997) ДНК-диагностика семейного случая спинальной и бульбарной амиотрофии Кеннеди. Журнал невропатологии и психиатрии им. С.С.Корсакова 97 (3): 45-48.
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10. Shah A.B., Chernov I., Zhang H.T., Ross B.M., Das K., Lutsenko S., Parano E., Pavone L., Evgrafov O., Ivanova-Smolenskaya I.A., Anneren G., Westermark K., Urrutia F.H., Penchaszaden G.K., Sternlieb I., Scheinberg I.H., Gilliam T.C., Petrukhin K. (1997) Identification and analysis of mutations in the Wilson disease gene (ATP7B): Population frequencies, genotype-phenotype correlation, and functional analyses. Am. J. H. Genet. 61: 317-328.
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11. Zelenin AV, Kolesnikov VA, Tarasenko OA, Shafei RA, Zelenina IA, Mikhailov VV, Semenova ML, Kovalenko DV, Artemyeva OV, Ivaschenko TE, Evgrafov OV, Dickson G, Baranov VS (1997) Bacterial beta-galactosidase and human dystrophin genes are expressed in mouse skeletal muscle fibers after ballistic transfection. FEBS Lett;414(2):319-322.
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PubMed]
12. Tverskaya SM, Dadali EL, Evgrafov OV (1997) Prenatal DNA diagnosis on demand--a possible new approach to DNA service provision. Prenat Diagn 1997 Oct;17(10):989-990.
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13. Gelfand MS, Pugachev VV, Evgrafov OV (1997) A new member of the MER2 repeat family is detected in the promoter region of the human X11 gene. Dokl Akad Nauk 1997 Jun;354(5):690-695.
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14. Polyakov A., Dzenis I., Baharev V., Evgrafov O.V. (1997) High frequency of a splice mutation in intron 2 of the 21-hydroxylase gene in Russia could be partly explained by a founder effect. Human mutation, Mutation in brief. #33 (1997) On-line, or Hum Mutat. 1998; (6): S53-S54.
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15. S.Tverskaya, E.Dadali, O.Evgrafov. Prenatal DNA diagnosis in case of any monogenic hereditary disease with localized gene: a possible concept for DNA service. 29 annual meeting of ESHG, Genova, Italy, May 1997, p 2-158.
16. A.Polyakov, S.Tverskaya, G.Osipova, I.Dzenis, V.Baharev, O.Evgrafov. Molecular study of 21-hydroxylase gene in groups of patients with polycistic ovary and Turner syndromes. 29 annual meeting of ESHG, Genova, Italy, May 1997, p 4-352.
17. S.Tverskaya, A.Polyakov, O.Evgrafov. Identification of recombination sites within the 21-hydroxylase gene (CYP21) in two patients with adrenal hyperplasia. 9 Jahrestagung der Gesellschaft fur Humangenetik, Innsbruck, April 1997, P10-69.
