CHROMOSOME ABNORMALITIES IN SPONTANEOUS ABORTIONS: APPLICATION OF MULTICOLOR FLUORESCENT IN SITU HYBRIDIZATION AND ORIGINAL DNA PROBES FOR CHROMOSOMES 1, 9, 13, 14, 16, 18, 21, 22, X AND Y
Vorsanova SG1,*, Kirilova EA2, Yurov YB3, Kolotii AD1, Monakhov VV3, Iourov IY3, Beresheva AK1
*Corresponding Author: : Professor Dr. Svetlana G. Vorsanova, Director of Molecular-Cytogenetic Laboratory of Neuropsychiatric Diseases, Institute of Pediatrics and Children Surgery, Russian Ministry of Health, Taldom¬skaya str 2, 127 412 Moscow, Russia; Tel.: +7-095-484-1948; Fax: +7-095-952-8940; E-mail: y_yurov@ yahoo.com
page: 49

REFERENCES

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2. Boue J, Boue A, Lazar P. Retrospective and pro­spective epidemiological studies of 1500 karyotyped spontaneous human abortions. Teratology 1975;12(1): 11-26.

3. Stephenson MD, Awartani KA, Robinson WP. Cytogenetic analysis of miscarriages from couples with recurrent miscarriage: a case control study. Hum Reprod 2002; 17(2): 446-451.

4. Strom CM, Ginsberg N, Applebaum M, Bogozi N, White M, Caffarelli M, Verlinsky Y. Analysis of 95 first-trimester spontaneous abortions by chorionic villus sam­pling and karyotype. J Assist Reprod Genet 1992; 9(5): 458-461.

5. Robinson WP, McFadden DE, Stephenson MD. The origin of abnormalities in recurrent aneuploidy/poly­ploidy. Am J Hum Genet 2001; 69(6): 1245-1254.

6. Causio F, Fischetto R, Sarcina E, Geusa S, Tartagni M. Chromosomal analysis of spontaneous abortions after in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI). Eur J Obstet Gynecol Reprod Biol 2002; 105(1): 44-48.

7. Bell KA, Van Deerlin PG, Haddad BR, Feinberg RF. Cytogenetic diagnosis of “normal 46,XX” karyotypes in spontaneous abortions frequently may be misleading. Fertil Steril 1999; 71(2): 334-341.

8. Jobanputra V, Sobrino A, Kinney A, Kline J, War­burton D. Multiplex interphase FISH as a screen for com­mon aneuploidies in spontaneous abortions. Hum Reprod 2002; 17(5): 1166-1170.

9. Rubio C, Simon C, Vidal F, Rodrigo L, Pehlivan T, Remonhi J, Pellicer A. Chromosomal abnormalities and embryo development in recurrent miscarriage couples. Hum Reprod 2003; 18(1): 182-188.


10. Yurov YB, Soloviev IV, Vorsanova SG, Marcais B, Roizes G, Lewis R. High resolution fluorescence in situ hybridization using cyanine and fluorescein dyes: ultra-rapid chromosome detection by directly fluorescently labeled alphoid DNA probes. Hum Genet 1996; 97(3): 390-398.

11. Soloviev IV, Yurov YB, Ioannou I, Georghiou A, Hadjimarcou M, Patsalis PC, Roizes G, Sharonin VO, Kravets VS, Vorsanova SG. Identification and molecular-cytogenetic characterization of large subsets of human plasmid, cosmids, PAC and YAC clones: the search of DNA probes for pre- and postnatal diagnosis. Cs Pediatr 1997; 52(7): 529-538.

12. Yurov YB, Vorsanova SG, Soloviev IV, Demi­dova IA, Alexandrov IA, Sharonin VO, Beresheva AK. Original collection of DNA probes for preimplantational, fetal prenatal and postnatal diagnosis of chromosomal analysis by FISH. In: Macek M Sr, Bianchi D, Cuckle H (eds). Early Prenatal Diagnosis, Fetal Cells and DNA in Mother, Present State and Perspectives. Prague: The Karolinum Press, 2002; 275-283.

13. Soloviev IV, Yurov YB, Vorsanova SG, Marcais B, Rogaev EI, Kapanadze BI, Brodiansky VM, Yan­kovsky NK, Roizes G. Fluorescent in situ hybridization analysis of a-satellite DNA in cosmid libraries specific for human chromosomes 13, 21 and 22. Rus J Genet 1998; 34(11): 1247-1255.




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