Medical Genetics - V. M. Zaporozhan 2005

References

PRIMARY LITERATURE

1. Bochkov, N. I. Clinical Genetics. — 2nd ed., rev. and enl. — M.: GEOTAR-MED, 2001. — 448 p.

2. Buzhiyevska, T. I. Fundamentals of Medical Genetics. — K.: Zdorovya, 2001. — 136 p.

3. Ginter, E. K. Medical Genetics: Textbook. — M.: Meditsina, 2003. — 448 p.

4. Clinical Genetics: Practical Training Manual / Yu. I. Bazhora, A. V. Shevelenkova, Z. N. Zhivats et al. — Odesa: Odesa State Medical University, 2001. — 146 p.

5. Reznik, B. Ya., Zaporozhan, V. N., Minkov, I. P. Congenital Malformations in Children. — Odesa: AO BAKHVA, 1994. — 448 p.

6. Hereditary diseases and Congenital Malformations in Perinatal Practice: Study Guide / V. M. Zaporozhan, A. M. Serdyuk, Yu. I. Bazhora et al. — K.: Zdorovya, 1997. — 360 p.

SUPPLEMENTARY LITERATURE

1. Ayala, F., Kiger, J. Modern Genetics: In 3 vols. / Transl. from English. — M.: Mir, 1987-1988.

2. Genome Analysis: Methods / G. Bunting, C. Cantor, F. Collins et al. / Ed. by K. Davies; Transl. from English. — M.: Mir, 1990. — 247 p.

3. Bazhora, Yu. I. Introduction to Immunogenetics: Lectures. — Odesa: OSMU, 2000. — 72 p.

4. Bazhora, Yu. I. Pharmacogenetics: Achievements and Perspectives. — Odesa: Druk, 2003. — 140 p.

5. Barashnev, Yu. I., Bakharev, V. A., & Novikov, P. V. (2004). Diagnosis and Treatment of congenital and hereditary diseases in children: A guide to clinical genetics. Moscow: Triada. 560 p.

6. Barilyak, I. R., Kovalchuk, L. E., & Skyban, G. V. (2000). Medical and Genetic explanatory dictionary. Ternopil: Ukrmedknyha. 376 p.

7. Benikova, E. A., Buzhiyevskaya, T. I., & Sylvanskaya, E. M. (1993). Genetics of endocrine diseases. Kyiv: Naukova Dumka. 400 p.

8. Bochkov, N. P., & Chebotarev, A. N. (1989). Human heredity and Environmental Mutagens. Moscow: Meditsina. 272 p.

9. Vakharlovsky, V. G., & Baranov, V. S. (2003). Hereditary diseases and prenatal Diagnostics. St. Petersburg: Znanie, IVESEP. 48 p.

10. Vorsanova, S. G., Yurov, Yu. B., & Chernyshov, V. N. (1999). Chromosomal syndromes and anomalies: Classification and Nomenclature. Rostov-on-Don: RGMU Publishing House. 192 p.

11. Simpson, J. L., Golbus, M. S., Martin, A. O., & Sarto, G. E. (1985). Genetics in obstetrics and gynecology (Trans. from English). Moscow: Meditsina. 352 p.

12. Barilyak, I. R., Buzhiyevskaya, T. I., Bykorez, A. I., et al. (1989). Genetic consequences of environmental pollution (T. I. Buzhiyevskaya, Ed.). Kyiv: Naukova Dumka. 229 p.

13. Baranov, V. S., Baranova, E. V., Ivashchenko, T. E., & Aseyev, M. V. (2000). The Human Genome and "predisposition" genes (Introduction to predictive medicine). St. Petersburg: Intermedika. 272 p.

14. Serdyuk, A. M., Tymchenko, O. I., Goyda, N. G., et al. (2003). Gene pool and population health: Methodology for assessing risk from environmental mutagens, directions for the Prevention of genetically determined pathologies. Kyiv: IGME AMS of Ukraine. 190 p.

15. Gershenzon, S. M. (1996). The diverse significance of Meiosis for problems of general biology. Kyiv: Naukova Dumka. 137 p.

16. Gershenzon, S. M. (1991). Mutations. Kyiv: Naukova Dumka. 112 p.

17. Gorbunova, V. N., & Baranov, V. S. (1997). Introduction to Molecular Diagnostics and Gene Therapy of hereditary diseases. St. Petersburg: Spetsialnaya Literatura. 287 p.

18. Grechanina, O. Y., & Grechanina, Y. B. (1998). Genomic Imprinting and imprinting disorders: Guidelines. Kharkiv, 15 p.

19. Zhegunov, G. F., Boyanovich, Y. V., & Zhegunova, G. P. (2002). Cytogenetic foundations of vital activity. Kharkiv, 406 p.

20. Zaporozhan, V. N., Aryayev, N. L., & Starets, E. A. (2001). Cystic fibrosis. Kyiv: Zdorovya, 176 p.

21. Zaporozhan, V. N., & Bazhora, Y. I. (2004). Stem Cells. Odesa: Odesa State Medical University, 228 p.

22. Zerova-Lyubimova, T. E., & Gorovenko, N. G. (2003). Standards for the analysis of human chromosome preparations: Guidelines. Kyiv, 52 p.

23. Zerova-Lyubimova, T. E., & Gorovenko, N. G. (2003). Cytogenetic Methods for human chromosome research: Guidelines. Kyiv, 23 p.

24. Illarioshkin, S. N., Ivanova-Smolenskaya, I. A., & Markova, E. D. (2002). DNA diagnostics and MEDICAL Genetic Counseling in neurology. Moscow: Meditsinskoe Informatsionnoe Agentstvo, 591 p.

25. Kadurina, T. I. (2000). Hereditary collagenopathies. Saint Petersburg: Nevsky Dialekt, 271 p.

26. Roisen, M. C., & Roth, K. S. (1986). Early diagnosis of inherited metabolic diseases. Moscow: Meditsina, 637 p.

27. Kopnin, B. P. (2000). Targets of oncogene and tumor suppressor action: Keys to understanding the mechanisms of carcinogenesis. Biochemistry, 65, 5–33.

28. Lazyuk, G. I., Lurie, I. V., & Cherstvoy, E. D. (1983). Hereditary syndromes of multiple congenital malformations. Moscow: Meditsina, 204 p.

29. Lilyin, E. T., Bogomazov, E. A., & Gofman-Kadoshnikov, P. B. (1990). Genetics for physicians. Moscow: Meditsina, 256 p.

30. METHODOLOGICAL GUIDELINES FOR Organizing Students' Independent Work in Clinical Genetics / V. T. Hermanov, O. M. Andrushchenko, I. V. Rudenko. — Luhansk: Luhansk State Medical University, 2003. — 88 p.

31. Mylytskyi V. F., Pishak V. P., Proniaiev V. I. Hereditary Syndromes: An Eponymic Dictionary and Handbook. — Chernivtsi: Prut, 1998. — 312 p.

32. Molecular Clinical Diagnosis: Methods: Translated from English / Edited by S. Harrington, J. McGee. — Moscow: Mir, 1999. — 558 p.

33. Mutovin G. R. Fundamentals of Clinical Genetics. — 2nd ed., rev. and enl. — Moscow: Vysshaya Shkola, 2001. — 234 p.

34. Mushkambarov N. N., Kuznetsov S. L. Molecular Biology: Textbook for Medical University Students. — Moscow: Medical Information Agency LLC, 2003. — 544 p.

35. Order of the Ministry of Health of Ukraine "On Improving Medical Genetic Care in Ukraine" No. 641/84 dated December 31, 2003. — Kyiv, 2003. — 104 p.

36. Human Hereditary Pathology: In 2 vols. / Edited by Yu. E. Veltishchev, N. P. Bochkov. — Moscow: Meditsina, 1992. — Vol. 1. — 276 p.; Vol. 2. — 245 p.

37. Hereditary Metabolic Disorders in Children: Diagnosis, Treatment, Prevention / Yu. I.

Barashnev, Yu. E. Veltishchev, V. P. Vetrov et al. // Medicine and Healthcare. Series: Medical Genetics and Immunology. — VNIIMI. — Moscow, 1984. — 66 p.

38. Hereditary Syndromes and Medical Genetic Counseling / S. I. Kozlova, N. S. Demikova, E. Semanova, O. E. Blinnikova. — Moscow: Meditsina, 1996. — 416 p.

39. Hereditary Systemic Skeletal Disorders / M. V. Volkov, E. M. Meerson, O. L. Nechvolodova et al. — Moscow: Meditsina, 1982. — 320 p.

40. Phenotype Description / L. V. Molodan, E. Bugaeva, O. O. Demina, I. V. Volchyk. — Kharkiv, 1998. — 49 p.

41. Puzyrev V. P., Stepanov V. A. Pathological Anatomy of the Human Genome. — Novosibirsk: Nauka, 1997. — 224 p.

42. Singer M., Berg P. Genes and Genomes. — Moscow: Mir, 1998. — Vol. 1. — 373 p.

43. Human Teratology: A Manual for Physicians / Ed. by G. I. Lazyuk. — Moscow: Meditsina, 1991. — 480 p.

44. Tymchenko O. I., Serdiuk A. M., Omelchenko E. M. Gene Pool and Public Health: The Significance of Marital Migrations. — Kyiv, 2002. — 79 p.

45. Totsky V. M. Genetics. — Odesa: Astroprint, 2002.

46. Vogel F., Motulsky A. Human Genetics: In 3 vols. / Transl. from English. — Moscow: Mir, 1989-1990.

47. Harper P. S. Practical Genetic Counselling / Transl. from English. — Moscow: Meditsina, 1989. — 304 p.

48. Human Chromosomes: An Atlas / A. F. Zakharov, V. A. Benyush, N. P. Kuleshov, L. I. Baranovskaya. — Moscow: Meditsina, 1982. — 264 p.

49. Shchipkov V. P., Krivoshein G. N. General and Medical Genetics. — Moscow: Akademiya, 2003. — 256 p.

50. Emery’s Elements of Medical Genetics / Robert F. Muller, Jan Young. — London, 2001. — 349 p.

51. Human Molecular Genetics / Tom Strachan, Andrew P. Read. — Bios Scientific Publishers, 1998. — 680 p.

52. Jones K. L. Smith’s Recognizable Patterns of Human Malformation: 5^th ed. — Philadelphia: W.B. Saunders, 1997.

53. Jorde Carey, Bamshad White Medical Genetics: 3^rd ed. — Elsevier (USA), 2003.

54. McKusick V. A. Mendelian Inheritance in Man. — 12^th ed. — Vol. 1-3. — Baltimore: Johns Hopkins University Press, 1998.