159 related articles for article (PubMed ID: 15284799)
21. Molecular cytogenetic evidence to characterize breakpoint regions in Robertsonian translocations.
Cheung SW; Sun L; Featherstone T
Cytogenet Cell Genet; 1990; 54(3-4):97-102. PubMed ID: 2265566
[TBL] [Abstract][Full Text] [Related]
22. Prenatal search for UPD 14 and UPD 15 in 83 cases of familial and de novo heterologous Robertsonian translocations.
Ruggeri A; Dulcetti F; Miozzo M; Grati FR; Grimi B; Bellato S; Natacci F; Maggi F; Simoni G
Prenat Diagn; 2004 Dec; 24(12):997-1000. PubMed ID: 15614836
[TBL] [Abstract][Full Text] [Related]
23. Evolution of the meiotic prophase and of the chromosome pairing process during human fetal ovarian development.
Roig I; Robles P; Garcia R; Martin M; Egozcue J; Cabero L; Barambio S; Garcia M
Hum Reprod; 2005 Sep; 20(9):2463-9. PubMed ID: 15905292
[TBL] [Abstract][Full Text] [Related]
24. An analysis of meiotic pairing in trisomy 21 oocytes using fluorescent in situ hybridization.
Cheng EY; Chen YJ; Bonnet G; Gartler SM
Cytogenet Cell Genet; 1998; 80(1-4):48-53. PubMed ID: 9678334
[TBL] [Abstract][Full Text] [Related]
25. Biparental inheritance of chromosome 21 polymorphic markers indicates that some Robertsonian translocations t(21;21) occur postzygotically.
Blouin JL; Binkert F; Antonarakis SE
Am J Med Genet; 1994 Feb; 49(3):363-8. PubMed ID: 8209906
[TBL] [Abstract][Full Text] [Related]
26. Interchromosomal effect in sperm of males with translocations: report of 6 cases and review of the literature.
Douet-Guilbert N; Bris MJ; Amice V; Marchetti C; Delobel B; Amice J; Braekeleer MD; Morel F
Int J Androl; 2005 Dec; 28(6):372-9. PubMed ID: 16300670
[TBL] [Abstract][Full Text] [Related]
27. 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
[TBL] [Abstract][Full Text] [Related]
28. A case of mosaic Down's syndrome with two Robertsonian translocations.
Leal-Garza CH; Cortés-Gutiérrez EI; Ortiz-Jalomo R; García-Cavazos R
Rev Invest Clin; 1996; 48(5):385-8. PubMed ID: 8968157
[TBL] [Abstract][Full Text] [Related]
29. Down syndrome due to de novo Robertsonian translocation t(14q;21q): DNA polymorphism analysis suggests that the origin of the extra 21q is maternal.
Petersen MB; Adelsberger PA; Schinzel AA; Binkert F; Hinkel GK; Antonarakis SE
Am J Hum Genet; 1991 Sep; 49(3):529-36. PubMed ID: 1831959
[TBL] [Abstract][Full Text] [Related]
30. Segregation of chromosomes into the spermatozoa of a man heterozygous for a 14;21 Robertsonian translocation.
Balkan W; Martin RH
Am J Med Genet; 1983 Oct; 16(2):169-72. PubMed ID: 6650563
[TBL] [Abstract][Full Text] [Related]
31. Human fetal ovarian culture permits meiotic progression and chromosome pairing process.
Roig I; Garcia R; Robles P; Cortvrindt R; Egozcue J; Smitz J; Garcia M
Hum Reprod; 2006 Jun; 21(6):1359-67. PubMed ID: 16449311
[TBL] [Abstract][Full Text] [Related]
32. Chromosome painting analysis of early oogenesis in human trisomy 18.
Cheng EY; Chen YJ; Gartler SM
Cytogenet Cell Genet; 1995; 70(3-4):205-10. PubMed ID: 7789172
[TBL] [Abstract][Full Text] [Related]
33. [Duration of meiotic prophase stages during oogenesis in the newt Triturus cristatus cristatus].
Safronov VV; Makarov VB
Ontogenez; 1976; 7(5):502-6. PubMed ID: 1036113
[TBL] [Abstract][Full Text] [Related]
34. [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
[TBL] [Abstract][Full Text] [Related]
35. Sperm fluorescence in situ hybridization analysis reveals normal sperm cells for 14;14 homologous male Robertsonian translocation carrier.
Cinar C; Beyazyurek C; Ekmekci CG; Aslan C; Kahraman S
Fertil Steril; 2011 Jan; 95(1):289.e5-9. PubMed ID: 20646694
[TBL] [Abstract][Full Text] [Related]
36. Influence of sex on the meiotic segregation of a t(13;17) Robertsonian translocation: a case study in the pig.
Pinton A; Calgaro A; Bonnet N; Ferchaud S; Billoux S; Dudez AM; Mary N; Massip K; Bonnet-Garnier A; Yerle M; Ducos A
Hum Reprod; 2009 Aug; 24(8):2034-43. PubMed ID: 19403564
[TBL] [Abstract][Full Text] [Related]
37. [Molecular genetics in chronic myeloid leukemia with variant Ph translocation].
Wu W; Li JY; Zhu Y; Qiu HR; Pan JL; Xu W; Chen LJ; Shen YF; Xue YQ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug; 24(4):470-3. PubMed ID: 17680547
[TBL] [Abstract][Full Text] [Related]
38. From spermatocytes to sperm: meiotic behaviour of human male reciprocal translocations.
Oliver-Bonet M; Navarro J; Codina-Pascual M; Abad C; Guitart M; Egozcue J; Benet J
Hum Reprod; 2004 Nov; 19(11):2515-22. PubMed ID: 15333594
[TBL] [Abstract][Full Text] [Related]
39. Prenatal detection of a de novo Yqh-acrocentric translocation.
Ng LK; Kwok YK; Tang LY; Ng PP; Ghosh A; Lau ET; Tang MH
Clin Biochem; 2006 Mar; 39(3):219-23. PubMed ID: 16515778
[TBL] [Abstract][Full Text] [Related]
40. The utility of interphase fluorescence in situ hybridization for the detection of the translocation t(11;14)(q13;q32) in the diagnosis of mantle cell lymphoma on fine-needle aspiration specimens.
Caraway NP; Gu J; Lin P; Romaguera JE; Glassman A; Katz R
Cancer; 2005 Apr; 105(2):110-8. PubMed ID: 15712276
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]