
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
1. Hassold T, Jacobs P. Trisomy in man. Annu Rev Genet 1984; 18: 69-97.
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.
|
|
|
|



 |
Number 27 VOL. 27 (2), 2024 |
Number 27 VOL. 27 (1), 2024 |
Number 26 Number 26 VOL. 26(2), 2023 All in one |
Number 26 VOL. 26(2), 2023 |
Number 26 VOL. 26, 2023 Supplement |
Number 26 VOL. 26(1), 2023 |
Number 25 VOL. 25(2), 2022 |
Number 25 VOL. 25 (1), 2022 |
Number 24 VOL. 24(2), 2021 |
Number 24 VOL. 24(1), 2021 |
Number 23 VOL. 23(2), 2020 |
Number 22 VOL. 22(2), 2019 |
Number 22 VOL. 22(1), 2019 |
Number 22 VOL. 22, 2019 Supplement |
Number 21 VOL. 21(2), 2018 |
Number 21 VOL. 21 (1), 2018 |
Number 21 VOL. 21, 2018 Supplement |
Number 20 VOL. 20 (2), 2017 |
Number 20 VOL. 20 (1), 2017 |
Number 19 VOL. 19 (2), 2016 |
Number 19 VOL. 19 (1), 2016 |
Number 18 VOL. 18 (2), 2015 |
Number 18 VOL. 18 (1), 2015 |
Number 17 VOL. 17 (2), 2014 |
Number 17 VOL. 17 (1), 2014 |
Number 16 VOL. 16 (2), 2013 |
Number 16 VOL. 16 (1), 2013 |
Number 15 VOL. 15 (2), 2012 |
Number 15 VOL. 15, 2012 Supplement |
Number 15 Vol. 15 (1), 2012 |
Number 14 14 - Vol. 14 (2), 2011 |
Number 14 The 9th Balkan Congress of Medical Genetics |
Number 14 14 - Vol. 14 (1), 2011 |
Number 13 Vol. 13 (2), 2010 |
Number 13 Vol.13 (1), 2010 |
Number 12 Vol.12 (2), 2009 |
Number 12 Vol.12 (1), 2009 |
Number 11 Vol.11 (2),2008 |
Number 11 Vol.11 (1),2008 |
Number 10 Vol.10 (2), 2007 |
Number 10 10 (1),2007 |
Number 9 1&2, 2006 |
Number 9 3&4, 2006 |
Number 8 1&2, 2005 |
Number 8 3&4, 2004 |
Number 7 1&2, 2004 |
Number 6 3&4, 2003 |
Number 6 1&2, 2003 |
Number 5 3&4, 2002 |
Number 5 1&2, 2002 |
Number 4 Vol.3 (4), 2000 |
Number 4 Vol.2 (4), 1999 |
Number 4 Vol.1 (4), 1998 |
Number 4 3&4, 2001 |
Number 4 1&2, 2001 |
Number 3 Vol.3 (3), 2000 |
Number 3 Vol.2 (3), 1999 |
Number 3 Vol.1 (3), 1998 |
Number 2 Vol.3(2), 2000 |
Number 2 Vol.1 (2), 1998 |
Number 2 Vol.2 (2), 1999 |
Number 1 Vol.3 (1), 2000 |
Number 1 Vol.2 (1), 1999 |
Number 1 Vol.1 (1), 1998 |
|
|