354 related articles for article (PubMed ID: 16343250)
1. Is cytogenetic diagnosis of 46,XX karyotype spontaneous abortion specimens erroneous? Fluorescence in situ hybridization as a confirmatory technique.
Karaoguz MY; Nas T; Konaç E; Ince D; Pala E; Menevse S
J Obstet Gynaecol Res; 2005 Dec; 31(6):508-13. PubMed ID: 16343250
[TBL] [Abstract][Full Text] [Related]
2. SRY gene amplifications and genotypings revealed the occurrence of the hidden maternal decidual cells in 46,XX karyotyped spontaneous abortions.
Karaoguz MY; Percin EF; Pala E; Biri AA; Korucuoglu U
Genet Couns; 2010; 21(1):9-17. PubMed ID: 20420024
[TBL] [Abstract][Full Text] [Related]
3. Cytogenetic analyses of culture failures by comparative genomic hybridisation (CGH)-Re-evaluation of chromosome aberration rates in early spontaneous abortions.
Fritz B; Hallermann C; Olert J; Fuchs B; Bruns M; Aslan M; Schmidt S; Coerdt W; Müntefering H; Rehder H
Eur J Hum Genet; 2001 Jul; 9(7):539-47. PubMed ID: 11464246
[TBL] [Abstract][Full Text] [Related]
4. A mathematical model for evaluation of maternal cell contamination in cultured cells from spontaneous abortions: significance for cytogenetic analysis of prenatal selection factors.
Nikitina TV; Lebedev IN; Sukhanova NN; Sazhenova EA; Nazarenko SA
Fertil Steril; 2005 Apr; 83(4):964-72. PubMed ID: 15820808
[TBL] [Abstract][Full Text] [Related]
5. [Molecular cytogenetic characteristics of chromosome imbalance in cells of spontaneous human abortion fetuses with low proliferative activity in vitro].
Lebedev IN; Ostroverkhova NV; Nikitina TV; Sukhanova NN; Nazarenko SA
Genetika; 2003 Aug; 39(8):1111-22. PubMed ID: 14515469
[TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs.
Giardino D; Corti C; Ballarati L; Finelli P; Valtorta C; Botta G; Giudici M; Grosso E; Larizza L
Prenat Diagn; 2006 Jun; 26(6):565-70. PubMed ID: 16683274
[TBL] [Abstract][Full Text] [Related]
7. [Maternal cell contamination of cultures of spontaneous abortion fibroblasts: importance for cytogenetic analysis of embryonic lethality].
Nikitina TV; Lebedev IN; Sukhanova NN; Sazhenova EA; Nazarenko SA
Genetika; 2004 Jul; 40(7):981-92. PubMed ID: 15458210
[TBL] [Abstract][Full Text] [Related]
8. [Marker chromosome analysis in Chinese patients with Turner syndrome by fluorescence in situ hybridization].
Liang Y; Luo XP
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):435-7. PubMed ID: 16086285
[TBL] [Abstract][Full Text] [Related]
9. Prenatal and postnatal characterization of Y chromosome structural anomalies by molecular cytogenetic analysis.
Hernando C; Carrera M; Ribas I; Parear N; Baraibar R; Egocue J; Fuster C
Prenat Diagn; 2002 Sep; 22(9):802-5. PubMed ID: 12224075
[TBL] [Abstract][Full Text] [Related]
10. [Genetic analysis of chorionic villi specimen in spontaneous abortion using various methods].
Lei Q; Wang Q; Zhou CQ; Chen BJ; Chen Z; Xu YW; Zeng YH
Zhonghua Fu Chan Ke Za Zhi; 2009 Apr; 44(4):253-6. PubMed ID: 19570460
[TBL] [Abstract][Full Text] [Related]
11. Cytogenetic analyses of premature ovarian failure using karyotyping and interphase fluorescence in situ hybridization (FISH) in a group of 1000 patients.
Lakhal B; Braham R; Berguigua R; Bouali N; Zaouali M; Chaieb M; Veitia RA; Saad A; Elghezal H
Clin Genet; 2010 Aug; 78(2):181-5. PubMed ID: 20345472
[TBL] [Abstract][Full Text] [Related]
12. [Delineating a supernumerary marker chromosome by combining several cytogenetic and molecular cytogenetic techniques].
Tan YQ; Di YF; Song YZ; Cheng DH; Li LY; Lu GX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):392-6. PubMed ID: 17680527
[TBL] [Abstract][Full Text] [Related]
13. [Molecular and cytogenetic study on 18 cases of amenorrhea: the use of fluorescence in situ hybridization and high resolution-comparative genomic hybridization].
Kong H; Ge YS; Wu Q; Wu HN; Zhou DX; Shen YY; Zheng YL; Cai MJ; Li J; Huang XL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Jun; 24(3):256-60. PubMed ID: 17557232
[TBL] [Abstract][Full Text] [Related]
14. Application of quantitative fluorescent PCR with short tandem repeat markers to the study of aneuploidies in spontaneous miscarriages.
Diego-Alvarez D; Garcia-Hoyos M; Trujillo MJ; Gonzalez-Gonzalez C; Rodriguez de Alba M; Ayuso C; Ramos-Corrales C; Lorda-Sanchez I
Hum Reprod; 2005 May; 20(5):1235-43. PubMed ID: 15760965
[TBL] [Abstract][Full Text] [Related]
15. [Cytogenetic studies of spontaneous abortions in humans].
Zhou CR
Zhonghua Fu Chan Ke Za Zhi; 1990 Mar; 25(2):89-91, 124. PubMed ID: 2364797
[TBL] [Abstract][Full Text] [Related]
16. [Non-radioactive in situ hybridization of alpha-satellite sequences in cytogenetic diagnosis].
Perfumo C; Arslanian A; Zara F; Piombo G; Pierluigi M
Pathologica; 1992; 84(1091):363-9. PubMed ID: 1465321
[TBL] [Abstract][Full Text] [Related]
17. Chromosome inversions and a novel chromosome insertion associated with recurrent miscarriages in South India.
Rao L; Murthy K; Babu A; Venkata P; Deenadayal M; Singh L
Arch Gynecol Obstet; 2005 Oct; 272(4):273-7. PubMed ID: 16021492
[TBL] [Abstract][Full Text] [Related]
18. [Spontaneous abortion: cytogenetic study of 609 cases].
Be C; Velásquez P; Youlton R
Rev Med Chil; 1997 Mar; 125(3):317-22. PubMed ID: 9460269
[TBL] [Abstract][Full Text] [Related]
19. [Application of fluorescence insitu hybridization technique for prenatal diagnosis of chromosome abnormality in amniotic cells].
Huang Y; Sun X; Li Q
Zhonghua Fu Chan Ke Za Zhi; 1999 Mar; 34(3):153-5. PubMed ID: 11263185
[TBL] [Abstract][Full Text] [Related]
20. Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesis.
Aktas D; Alikasifoglu M; Gonc N; Senocak ME; Tuncbilek E
Eur J Med Genet; 2006; 49(2):141-9. PubMed ID: 16530711
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
