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Similar articles for PubMed (Select 24434955)

1.

Chromosome 16 abnormalities in embryos and in sperm from a male with a fragile site at 16q22.1.

Martorell MR, Martínez-Pasarell O, Lopez O, Polo A, Sandalinas M, Garcia-Guixé E, Bassas L.

Cytogenet Genome Res. 2014;142(2):134-9. doi: 10.1159/000357411. Epub 2014 Jan 14.

PMID:
24434955
2.

Single-nucleotide polymorphism microarray-based preimplantation genetic diagnosis is likely to improve the clinical outcome for translocation carriers.

Tan YQ, Tan K, Zhang SP, Gong F, Cheng DH, Xiong B, Lu CF, Tang XC, Luo KL, Lin G, Lu GX.

Hum Reprod. 2013 Sep;28(9):2581-92. doi: 10.1093/humrep/det271. Epub 2013 Jul 11.

3.

Chromosome segregation analysis in human embryos obtained from couples involving male carriers of reciprocal or Robertsonian translocation.

Yilmaz A, Zhang XY, Chung JT, Tan SL, Holzer H, Ao A.

PLoS One. 2012;7(9):e46046. doi: 10.1371/journal.pone.0046046. Epub 2012 Sep 27.

4.

Prenatal detection of del(10)(q11.2) mosaicism in chorionic villus specimens likely caused by a common chromosomal fragile site FRA10G is associated with a normal phenotype.

Liao J, Sathanoori M, Yatsenko SA, Hu J, Kochmar SJ, Hoffner L, Hogge WA, Surti U.

Prenat Diagn. 2012 Dec;32(12):1166-9. doi: 10.1002/pd.3977. Epub 2012 Sep 26.

PMID:
23015528
5.

Normal birth following PGD for reciprocal translocation after serial vitrification of oocytes from a poor responder: a case report.

Chung JT, Son WY, Zhang XY, Ao A, Tan SL, Holzer H.

Reprod Biomed Online. 2012 Nov;25(5):521-6. doi: 10.1016/j.rbmo.2012.07.017. Epub 2012 Aug 6.

PMID:
22995749
6.

Spontaneous expression of FRA16B in a non-consanguineous couple experiencing multiple fetal losses.

Aswini S, Jegatheesan T, Chandra N.

J Obstet Gynaecol Res. 2012 Sep;38(9):1223-7. doi: 10.1111/j.1447-0756.2012.01850.x. Epub 2012 May 8.

PMID:
22564372
7.

Normal sperm in a 2;2 homologous male translocation carrier.

Almeida C, Dória S, Moreira M, Pinto J, Barros A.

J Assist Reprod Genet. 2012 Jul;29(7):665-8. doi: 10.1007/s10815-012-9770-6. Epub 2012 Apr 27.

8.

The effect of the swim-up and hyaluronan-binding methods on the frequency of abnormal spermatozoa detected by FISH and SCSA in carriers of balanced chromosomal translocations.

Vozdova M, Kasikova K, Oracova E, Prinosilova P, Rybar R, Horinova V, Gaillyova R, Rubes J.

Hum Reprod. 2012 Mar;27(3):930-7. doi: 10.1093/humrep/der445. Epub 2012 Jan 11.

9.

Chromosome breakage in human preimplantation embryos from carriers of structural chromosomal abnormalities in relation to fragile sites, maternal age, and poor sperm factors.

Xanthopoulou L, Ghevaria H, Mantzouratou A, Serhal P, Doshi A, Delhanty JD.

Cytogenet Genome Res. 2012;136(1):21-9. doi: 10.1159/000334836. Epub 2011 Dec 14.

PMID:
22179562
10.

Jacobsen syndrome due to an unbalanced translocation between 11q23 and 22q11.2 identified at age 40 years.

Takahashi I, Takahashi T, Sawada K, Shimojima K, Yamamoto T.

Am J Med Genet A. 2012 Jan;158A(1):220-3. doi: 10.1002/ajmg.a.34382. Epub 2011 Dec 2.

PMID:
22139980
11.

Chromosome analysis by spectral karyotyping of spermatozoa from an oligoasthenozoospermic carrier of a 10; 21 reciprocal translocation.

Motoyama M, Takahashi K, Ogawa S, Ohno M, Yoshizawa M, Fukui E, Araki S.

Hum Cell. 2011 Dec;24(4):146-9. doi: 10.1007/s13577-011-0035-y. Epub 2011 Oct 12.

PMID:
21989793
12.

Impact of reciprocal translocation t (18; 21) on male infertility and embryo development: lessons from an oocyte-donating ICSI cycle.

Gu L, Zhang H, Zhu G.

J Assist Reprod Genet. 2011 Jul;28(7):603-5. doi: 10.1007/s10815-011-9558-0. Epub 2011 Apr 1.

13.

First successful pregnancy following PGD for chromosome translocation on embryos generated from in-vitro matured oocytes: a case report.

Ao A, Zhang XY, Tan SL.

Reprod Biomed Online. 2011 Apr;22(4):371-5. doi: 10.1016/j.rbmo.2010.11.014. Epub 2010 Nov 25.

PMID:
21324743
14.

Aneuploidies in embryos and spermatozoa from patients with Y chromosome microdeletions.

Mateu E, Rodrigo L, Martínez MC, Peinado V, Milán M, Gil-Salom M, Martínez-Jabaloyas JM, Remohí J, Pellicer A, Rubio C.

Fertil Steril. 2010 Dec;94(7):2874-7. doi: 10.1016/j.fertnstert.2010.06.046. Epub 2010 Jul 24.

PMID:
20655521
15.

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 1;93(7):2413.e1-5. doi: 10.1016/j.fertnstert.2009.12.032. Epub 2010 Feb 1.

PMID:
20117768
16.

[Application of sperm fluorescence in situ hybridization in preimplantation genetic diagnosis].

Li G, Sun YP, Jin HX, Xin ZM, Dai SJ.

Zhonghua Fu Chan Ke Za Zhi. 2009 Jun;44(6):418-21. Chinese.

PMID:
19953940
17.

Characteristics of embryo development in Robertsonian translocations' preimplantation genetic diagnosis cycles.

Huang J, Lian Y, Qiao J, Chen Y, Ren X, Liu P.

Prenat Diagn. 2009 Dec;29(12):1167-70. doi: 10.1002/pd.2376.

PMID:
19813217
18.

Sperm meiotic segregation and aneuploidy in a 46,X,inv(Y),t(10;15) carrier: case report.

Vozdova M, Oracova E, Gaillyova R, Rubes J.

Fertil Steril. 2009 Nov;92(5):1748.e9-13. doi: 10.1016/j.fertnstert.2009.08.020. Epub 2009 Sep 4.

PMID:
19733349
19.
20.
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