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Items: 1 to 20 of 99

1.

Familial complex chromosome rearrangement (CCR) involving 5 breakpoints on chromosomes 1, 3 and 13 in a severe oligozoospermic patient.

Li L, Heng X, Yun W, Zheng S, Zhang J, Fan W.

J Assist Reprod Genet. 2013 Mar;30(3):423-9. doi: 10.1007/s10815-013-9934-z. Epub 2013 Feb 5. No abstract available.

2.

De novo complex chromosome rearrangement: a study of two patients.

Melo DG, Huber J, Giuliani LR, Mazzucatto LF, Riegel M, Pina-Neto JM.

Genet Couns. 2004;15(3):303-10.

PMID:
15517822
3.

Familial complex chromosomal rearrangement resulting in a recombinant chromosome.

Berend SA, Bodamer OA, Shapira SK, Shaffer LG, Bacino CA.

Am J Med Genet. 2002 May 15;109(4):311-7.

PMID:
11992486
4.

Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping.

Peschka B, Leygraaf J, Hansmann D, Hansmann M, Schröck E, Ried T, Engels H, Schwanitz G, Schubert R.

Prenat Diagn. 1999 Dec;19(12):1143-9. Review.

PMID:
10590433
5.

De novo double translocation 3;13 and 4;8;18 in a patient with mental retardation and skeletal abnormalities.

Battisti C, Bonaglia MC, Giglio S, Anichini C, Pucci L, Dotti MT, Zuffardi O, Federico A.

Am J Med Genet A. 2003 Mar 15;117A(3):207-11.

PMID:
12599183
6.

A de novo complex chromosome rearrangement involving three chromosomes (2, 13, and 18) in an oligospermic male.

Ergul E, Liehr T, Mrasek K, Sazci A.

Fertil Steril. 2009 Jul;92(1):391.e9-391.e12. doi: 10.1016/j.fertnstert.2009.02.042. Epub 2009 Apr 14.

PMID:
19368909
7.

A case with balanced chromosome rearrangement involving chromosomes 9, 14, and 13 in a woman with recurrent abortion.

Kim SK, Kim HJ, Yang YH, Kim IK, Bai SW, Kim JY, Park KH, Cho DJ, Song CH.

Yonsei Med J. 2001 Jun;42(3):345-8.

8.

Sperm FISH analysis of a 46,XY,t(3;6)(p24;p21.2),inv (8)(p11;2q21.2) double chromosomal rearrangement.

Ferfouri F, Boitrelle F, Tapia S, Molina Gomes D, Selva J, Vialard F.

Reprod Biomed Online. 2012 Feb;24(2):219-23. doi: 10.1016/j.rbmo.2011.10.009. Epub 2011 Oct 25.

PMID:
22196892
9.

High frequency of XY disomy in spermatozoa of severe oligozoospermic men.

Ohashi Y, Miharu N, Honda H, Samura O, Ohama K.

Hum Reprod. 2001 Apr;16(4):703-8.

PMID:
11278222
10.
11.

Complex chromosomal rearrangement involving chromosomes 1, 4 and 22 in an infertile male: case report and literature review.

Salahshourifar I, Shahrokhshahi N, Tavakolzadeh T, Beheshti Z, Gourabi H.

J Appl Genet. 2009;50(1):69-72. doi: 10.1007/BF03195655.

PMID:
19193986
12.

Alternative centromeric inactivation in a pseudodicentric t(Y;13)(q12;p11.2) translocation chromosome associated with extreme oligozoospermia.

Siffroi JP, Benzacken B, Angelopoulou R, Le Bourhis C, Berthaut I, Kanafani S, Smahi A, Wolf JP, Dadoune JP.

J Med Genet. 2001 Nov;38(11):802-6. No abstract available.

13.
14.

Complex chromosomal rearrangement and intracytoplasmic sperm injection: a case report.

Joly-Helas G, de La Rochebrochard C, Mousset-Siméon N, Moirot H, Tiercin C, Romana SP, Le Caignec C, Clavier B, Macé B, Rives N.

Hum Reprod. 2007 May;22(5):1292-7. Epub 2007 Feb 5.

PMID:
17283038
15.

[Meiotic analysis of spermatogenic cells in severe oligoasthenoteratozoospermia with chromosome 13 rearrangement].

Cui YX, Yang XY, Xia XY, Zhou Y, Chen YH, Hu YA.

Zhonghua Nan Ke Xue. 2012 Sep;18(9):793-6. Chinese.

PMID:
23193665
16.

Exploring the relationship between the severity of oligozoospermia and the frequencies of sperm chromosome aneuploidies.

Durak Aras B, Aras I, Can C, Toprak C, Dikoglu E, Bademci G, Ozdemir M, Cilingir O, Artan S.

Andrologia. 2012 Dec;44(6):416-22. doi: 10.1111/j.1439-0272.2012.01298.x. Epub 2012 Apr 27.

PMID:
22536802
17.

FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16.

Phelan MC, Blackburn W, Rogers RC, Crawford EC, Cooley NR Jr, Schrock E, Ning Y, Ried T.

Prenat Diagn. 1998 Nov;18(11):1174-80.

PMID:
9854728
18.

An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype.

Bartels I, Starke H, Argyriou L, Sauter SM, Zoll B, Liehr T.

Eur J Med Genet. 2007 Mar-Apr;50(2):133-8. Epub 2006 Nov 10.

PMID:
17174164
19.

Absolute polymorphic teratozoospermia in patients with oligo-asthenozoospermia is associated with an elevated sperm aneuploidy rate.

Vicari E, de Palma A, Burrello N, Longo G, Grazioso C, Barone N, Zahi M, D'Agata R, Calogero AE.

J Androl. 2003 Jul-Aug;24(4):598-603.

20.

De novo highly complex chromosome rearrangement (CCR) involving five breakpoints with congenital anomalies analyzed by FISH.

Curotti G, Benkhalifa M, Raybaud C, Picard F, Bellec V, Qumsiyeh MB.

Genet Couns. 1999;10(3):259-64.

PMID:
10546097

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