These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
138 related items for PubMed ID: 9949445
1. Case report: chromatid exchange and predivision of chromatids as other sources of abnormal oocytes detected by preimplantation genetic diagnosis of translocations. Munné S, Bahçe M, Schimmel T, Sadowy S, Cohen J. Prenat Diagn; 1998 Dec; 18(13):1450-8. PubMed ID: 9949445 [Abstract] [Full Text] [Related]
2. Successful pregnancy after preimplantation genetic diagnosis for carrier of t(2;7)(p11.2;q22) with high rates of unbalanced sperm and embryos: a case report. Wiland E, Hobel CJ, Hill D, Kurpisz M. Prenat Diagn; 2008 Jan; 28(1):36-41. PubMed ID: 18186141 [Abstract] [Full Text] [Related]
3. Analysis of nine chromosome probes in first polar bodies and metaphase II oocytes for the detection of aneuploidies. Pujol A, Boiso I, Benet J, Veiga A, Durban M, Campillo M, Egozcue J, Navarro J. Eur J Hum Genet; 2003 Apr; 11(4):325-36. PubMed ID: 12700606 [Abstract] [Full Text] [Related]
4. [The clinical application of whole chromosome painting probes in preimplantation genetic diagnosis for translocation carriers]. Ren XL, Xu YW, Zhuang GL, Zhou CQ, Liu Y, Ou JP, Li SP. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Apr; 24(2):140-3. PubMed ID: 17407068 [Abstract] [Full Text] [Related]
5. Female gamete segregation in two carriers of translocations involving 2q and 14q. Escudero T, Lee M, Sandalinas M, Munné S. Prenat Diagn; 2000 Mar; 20(3):235-7. PubMed ID: 10719328 [Abstract] [Full Text] [Related]
7. [Preimplantation genetic diagnosis of chromosome abnormality by fluorescence in-situ hybridization]. Xu CM, Jin F, Qian YL, Ye YH, Zhu YM, Huang HF. Zhonghua Fu Chan Ke Za Zhi; 2004 Jul; 39(7):453-6. PubMed ID: 15347467 [Abstract] [Full Text] [Related]
8. Sequential FISH analysis of oocytes and polar bodies reveals aneuploidy mechanisms. Cupisti S, Conn CM, Fragouli E, Whalley K, Mills JA, Faed MJ, Delhanty JD. Prenat Diagn; 2003 Aug; 23(8):663-8. PubMed ID: 12913873 [Abstract] [Full Text] [Related]
9. Meiotic and mitotic nondisjunction: lessons from preimplantation genetic diagnosis. Kuliev A, Verlinsky Y. Hum Reprod Update; 2004 Aug; 10(5):401-7. PubMed ID: 15319376 [Abstract] [Full Text] [Related]
10. Preimplantation genetic diagnosis (PGD) for extremes--successful birth after PGD for a consanguineous couple carrying an identical balanced reciprocal translocation. Beyazyurek C, Ekmekci CG, Sağlam Y, Cinar C, Kahraman S. Fertil Steril; 2010 May 01; 93(7):2413.e1-5. PubMed ID: 20117768 [Abstract] [Full Text] [Related]
11. Estimation of chromosomal imbalances in preimplantation embryos from preimplantation genetic diagnosis cycles of reciprocal translocations with or without acrocentric chromosomes. Lim CK, Cho JW, Song IO, Kang IS, Yoon YD, Jun JH. Fertil Steril; 2008 Dec 01; 90(6):2144-51. PubMed ID: 18440525 [Abstract] [Full Text] [Related]
12. Elucidation of abnormal fertilization by single-cell analysis with fluorescence in situ hybridization and polymorphic marker analysis. Malcov M, Frumkin T, Shwartz T, Azem F, Amit A, Yaron Y, Ben-Yosef D. Fertil Steril; 2009 Mar 01; 91(3):932.e3-6. PubMed ID: 19110241 [Abstract] [Full Text] [Related]
13. [Study on the mechanism of oocyte aneuploidy formation by multicolor fluorescence in situ hybridization]. Chen W, Mettler L. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Jun 01; 21(3):203-6. PubMed ID: 15192817 [Abstract] [Full Text] [Related]
14. Preimplantation genetic diagnosis for an insertional translocation carrier. Melotte C, Debrock S, D'Hooghe T, Fryns JP, Vermeesch JR. Hum Reprod; 2004 Dec 01; 19(12):2777-83. PubMed ID: 15471933 [Abstract] [Full Text] [Related]
15. Efficacy and clinical outcome of preimplantation genetic diagnosis using FISH for couples of reciprocal and Robertsonian translocations: the Korean experience. Kyu Lim C, Hyun Jun J, Mi Min D, Lee HS, Young Kim J, Koong MK, Kang IS. Prenat Diagn; 2004 Jul 01; 24(7):556-61. PubMed ID: 15300749 [Abstract] [Full Text] [Related]
16. Sperm segregation analysis of a (13;22) Robertsonian translocation carrier by FISH: a comparison of locus-specific probe and whole chromosome painting. Anahory T, Hamamah S, Andréo B, Hédon B, Claustres M, Sarda P, Pellestor F. Hum Reprod; 2005 Jul 01; 20(7):1850-4. PubMed ID: 15845597 [Abstract] [Full Text] [Related]
17. Using BAC clones to characterize unbalanced chromosome abnormalities in interphase cells. Plastira K, Maher E, Fantes J, Ramsay J, Angelopoulou R. Eur J Med Genet; 2006 Jul 01; 49(3):235-46. PubMed ID: 16762825 [Abstract] [Full Text] [Related]
18. Rare Robertsonian translocations and meiotic behaviour: sperm FISH analysis of t(13;15) and t(14;15) translocations: a case report. Moradkhani K, Puechberty J, Bhatt S, Lespinasse J, Vago P, Lefort G, Sarda P, Hamamah S, Pellestor F. Hum Reprod; 2006 Dec 01; 21(12):3193-8. PubMed ID: 16917122 [Abstract] [Full Text] [Related]
19. Fluorescence in situ hybridization analysis of human oocytes: advantages of a double-labeling procedure. Pellestor F, Anahory T, Andréo B, Régnier-Vigouroux G, Soulié JP, Baudouin M, Demaille J. Fertil Steril; 2004 Oct 01; 82(4):919-22. PubMed ID: 15482769 [Abstract] [Full Text] [Related]
20. Reliability of comparative genomic hybridization to detect chromosome abnormalities in first polar bodies and metaphase II oocytes. Gutiérrez-Mateo C, Wells D, Benet J, Sánchez-García JF, Bermúdez MG, Belil I, Egozcue J, Munné S, Navarro J. Hum Reprod; 2004 Sep 01; 19(9):2118-25. PubMed ID: 15271867 [Abstract] [Full Text] [Related] Page: [Next] [New Search]