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PUBMED FOR HANDHELDS

Journal Abstract Search


140 related items for PubMed ID: 31710435

  • 1. A Case of Complex Chromosome Translocation: 46, XY, t(4; 10; 13) (q31; q23; q12).
    Wang K, Zhao X, Tu H, Lin H.
    Clin Lab; 2019 Nov 01; 65(11):. PubMed ID: 31710435
    [Abstract] [Full Text] [Related]

  • 2. A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q13-->q24.1 and partial monosomy 4q27-->q28 [corrected].
    Grasshoff U, Singer S, Liehr T, Starke H, Fode B, Schöning M, Dufke A.
    Cytogenet Genome Res; 2003 Nov 01; 103(1-2):17-23. PubMed ID: 15004458
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  • 3. [Characteristics of complex chromosomal rearrangement in Chinese male carriers and its impact on male fertility].
    Chen YJ, Zhang WW, Wu YH, Sun XM, Bao H, Hu CJ.
    Zhonghua Nan Ke Xue; 2014 Dec 01; 20(12):1120-5. PubMed ID: 25597181
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  • 4. [A complex chromosome translocation with male infertility of karyotype analysis and literature review].
    Wu GJ, Ma S, Zheng LW, Xu Y, Meng FH, Dai XW.
    Beijing Da Xue Xue Bao Yi Xue Ban; 2018 Aug 18; 50(4):729-731. PubMed ID: 30122779
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  • 5. A de novo complex chromosomal rearrangement with a translocation 7;9 and 8q insertion in a male carrier with no infertility.
    Cai T, Yu P, Tagle DA, Lu D, Chen Y, Xia J.
    Hum Reprod; 2001 Jan 18; 16(1):59-62. PubMed ID: 11139537
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  • 7. Pregnancy outcome when both members of a couple have balanced translocations.
    Campbell SA, Uhlmann WR, Duquette D, Johnson MP, Evans MI.
    Obstet Gynecol; 1995 May 18; 85(5 Pt 2):844-6. PubMed ID: 7724133
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  • 8. Trisomy 4 pter-q12 and monosomy of chromosome 13 pter-q12 in a male with deficiency of all blood lymphocyte populations.
    Velagaleti GV, Lockhart LH, Schmalstieg FC, Goldman AS.
    Am J Med Genet; 2001 Aug 01; 102(2):139-45. PubMed ID: 11477605
    [Abstract] [Full Text] [Related]

  • 9. A Case of Rare Complex Translocation of four Chromosomes with Primary Infertility.
    Wang K, Tu H, Lin H, Xu G, Lun Y.
    Clin Lab; 2022 Nov 01; 68(11):. PubMed ID: 36377994
    [Abstract] [Full Text] [Related]

  • 10. Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection.
    Chen Z, Grebe TA, Guan XY, Notohamiprodjo M, Nutting PJ, Stone JF, Trent JM, Sandberg AA.
    Am J Med Genet; 1997 Aug 08; 71(2):160-6. PubMed ID: 9217215
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  • 11. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP, Chern SR, Lee CC, Lin CC, Li YC, Hsieh LJ, Chen WL, Wang W.
    Prenat Diagn; 2006 Feb 08; 26(2):138-46. PubMed ID: 16470734
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  • 15. Cytogenetic analysis in 61 couples with spontaneous abortions.
    Jiang J, Fu M, Wang D.
    Chin Med J (Engl); 2001 Feb 08; 114(2):200-1. PubMed ID: 11780207
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  • 18. 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 08; 29(7):665-8. PubMed ID: 22538551
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  • 19. Meiotic studies in two human reciprocal translocations and their association with spermatogenic failure.
    Oliver-Bonet M, Benet J, Sun F, Navarro J, Abad C, Liehr T, Starke H, Greene C, Ko E, Martin RH.
    Hum Reprod; 2005 Mar 08; 20(3):683-8. PubMed ID: 15689348
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