284 related articles for article (PubMed ID: 16155075)
1. Preimplantation genetic screening reveals a high incidence of aneuploidy and mosaicism in embryos from young women undergoing IVF.
Baart EB; Martini E; van den Berg I; Macklon NS; Galjaard RJ; Fauser BC; Van Opstal D
Hum Reprod; 2006 Jan; 21(1):223-33. PubMed ID: 16155075
[TBL] [Abstract][Full Text] [Related]
2. Re-analysis by fluorescence in situ hybridisation of spare embryos cultured until Day 5 after preimplantation genetic diagnosis for a 47, XYY infertile patient demonstrates a high incidence of diploid mosaic embryos: a case report.
Emiliani S; Merino EG; Van den Bergh M; Abramowicz M; Vassart G; Englert Y; Delneste D
Prenat Diagn; 2000 Dec; 20(13):1063-6. PubMed ID: 11180230
[TBL] [Abstract][Full Text] [Related]
3. Preimplantation genetic diagnosis for aneuploidy screening in early human embryos: a review.
Wilton L
Prenat Diagn; 2002 Jun; 22(6):512-8. PubMed ID: 12116318
[TBL] [Abstract][Full Text] [Related]
4. [Preliminary analysis of chromosome mosaicism in preimplantation embryos].
Xu Y; Zhuang G; Shu Y
Zhonghua Fu Chan Ke Za Zhi; 2000 Aug; 35(8):456-8. PubMed ID: 11776195
[TBL] [Abstract][Full Text] [Related]
5. Confirmation of diagnosis in preimplantation genetic diagnosis (PGD) through blastocyst culture: preliminary experience.
Veiga A; Gil Y; Boada M; Carrera M; Vidal F; Boiso I; Ménézo Y; Barri PN
Prenat Diagn; 1999 Dec; 19(13):1242-7. PubMed ID: 10660961
[TBL] [Abstract][Full Text] [Related]
6. Preimplantation genetic diagnosis of aneuploidy and male infertility.
Gianaroli L; Munné S; Magli MC; Ferraretti AP
Int J Androl; 1997; 20 Suppl 3():31-4. PubMed ID: 9466183
[TBL] [Abstract][Full Text] [Related]
7. Chromosomal diagnosis in each individual blastomere of 5- to 10-cell bovine embryos derived from in vitro fertilization.
Yoshizawa M; Konno H; Zhu S; Kageyama S; Fukui E; Muramatsu S; Kim S; Araki Y
Theriogenology; 1999 May; 51(7):1239-50. PubMed ID: 10729088
[TBL] [Abstract][Full Text] [Related]
8. Highly abnormal cleavage divisions in preimplantation embryos from translocation carriers.
Iwarsson E; Malmgren H; Inzunza J; Ahrlund-Richter L; Sjöblom P; Rosenlund B; Fridström M; Hovatta O; Nordenskjöld M; Blennow E
Prenat Diagn; 2000 Dec; 20(13):1038-47. PubMed ID: 11180227
[TBL] [Abstract][Full Text] [Related]
9. Assessment of numeric abnormalities of X, Y, 18, and 16 chromosomes in preimplantation human embryos before transfer.
Munné S; Sultan KM; Weier HU; Grifo JA; Cohen J; Rosenwaks Z
Am J Obstet Gynecol; 1995 Apr; 172(4 Pt 1):1191-9; discussion 1199-201. PubMed ID: 7726256
[TBL] [Abstract][Full Text] [Related]
10. [Dual color fluorescent in-situ hybridization detects sex chromosome mosaicism in human embryos].
Xu Y; Zhuang G; Zhou C
Zhonghua Fu Chan Ke Za Zhi; 1999 Oct; 34(10):603-5. PubMed ID: 11477799
[TBL] [Abstract][Full Text] [Related]
11. Relationship between morphology and chromosomal constitution in human preimplantation embryo.
Pellestor F; Girardet A; Andréo B; Arnal F; Humeau C
Mol Reprod Dev; 1994 Oct; 39(2):141-6. PubMed ID: 7826614
[TBL] [Abstract][Full Text] [Related]
12. [Detecting embryo sex by fluorescence in-situ hybridization in preimplantation genetic diagnosis].
Xu Y; Zhuang G; Li M
Zhonghua Fu Chan Ke Za Zhi; 2000 Aug; 35(8):465-7. PubMed ID: 11776198
[TBL] [Abstract][Full Text] [Related]
13. Chromosome analysis of human preimplantation embryos.
Carrera M; Veiga A
Croat Med J; 1998 Jun; 39(2):121-7. PubMed ID: 9575266
[TBL] [Abstract][Full Text] [Related]
14. Preimplantation genetic diagnosis of chromosomal abnormalities by multicolour fluorescence in situ hybridisation.
Parikh FR; Madon PF; Athalye AS; Naik NJ; Gada SD; Ganla KN; Nadkarni SG; Patki AS; Khot SS
J Indian Med Assoc; 2001 Aug; 99(8):441-4. PubMed ID: 11881859
[TBL] [Abstract][Full Text] [Related]
15. Chromosome 18 analysis by fluorescence in situ hybridization (FISH) in human blastomeres of abnormal embryos after in vitro fertilization (IVF) attempt.
Bergere M; Selva J; Baud M; Volante M; Martin B; Hugues JN; Olivennes F; Frydman R; Auroux M
Prenat Diagn; 1995 Sep; 15(9):835-41. PubMed ID: 8559754
[TBL] [Abstract][Full Text] [Related]
16. Supernumerary human preembryos provide potential for preimplantation genetic diagnosis.
Delimitreva SM; Zhivkova RS; Vatev IT
Folia Biol (Praha); 2001; 47(3):88-91. PubMed ID: 11409319
[TBL] [Abstract][Full Text] [Related]
17. Aneuploidy 16 in human embryos increases significantly with maternal age.
Benadiva CA; Kligman I; Munné S
Fertil Steril; 1996 Aug; 66(2):248-55. PubMed ID: 8690111
[TBL] [Abstract][Full Text] [Related]
18. Preimplantation genetic diagnosis increases the implantation rate in human in vitro fertilization by avoiding the transfer of chromosomally abnormal embryos.
Gianaroli L; Magli MC; Ferraretti AP; Fiorentino A; Garrisi J; Munné S
Fertil Steril; 1997 Dec; 68(6):1128-31. PubMed ID: 9418710
[TBL] [Abstract][Full Text] [Related]
19. Will preimplantation genetic diagnosis assist patients with a poor prognosis to achieve pregnancy?
Gianaroli L; Magli MC; Munné S; Fiorentino A; Montanaro N; Ferraretti AP
Hum Reprod; 1997 Aug; 12(8):1762-7. PubMed ID: 9308808
[TBL] [Abstract][Full Text] [Related]
20. Cytogenetics in reproductive medicine: the contribution of comparative genomic hybridization (CGH).
Wells D; Levy B
Bioessays; 2003 Mar; 25(3):289-300. PubMed ID: 12596234
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
