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Journal Abstract Search

323 related items for PubMed ID: 9039997

  • 21. [A case of partial trisomy 9pter --> q13 due to paternal balanced translocation t (9;21) (q13;q21)].
    Woo KS, Kim KE, Kwon EY, Kim JP, Han JY.
    Korean J Lab Med; 2008 Apr; 28(2):155-9. PubMed ID: 18458513
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  • 22. Familial cryptic (20;21) translocation identified by in situ hybridization technologies.
    Leppig KA, Ball S, Au K, Opheim KE, Norwood T.
    Am J Med Genet; 2000 Aug 14; 93(4):273-7. PubMed ID: 10946352
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  • 23. [Combined use of molecular cytogenetic techniques to detect a small chromosomal translocation].
    Xie YJ, Chen BJ, Wu JZ, Chen Z, Lin SB, Fang Q.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Oct 14; 28(5):568-71. PubMed ID: 21983737
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  • 24. Prenatal diagnosis of partial trisomy 22 derived from a maternal t(11; 22) (q23; q11).
    Sou S, Takabayashi T, Sasaki H, Sasamoto K, Shintaku Y, Li ZJ, Ozawa N, Yajima A.
    Tohoku J Exp Med; 1987 Dec 14; 153(4):389-93. PubMed ID: 3441929
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  • 25. Meiotic studies of a human male carrier of the common translocation, t(11;22), suggests postzygotic selection rather than preferential 3:1 MI segregation as the cause of liveborn offspring with an unbalanced translocation.
    Armstrong SJ, Goldman AS, Speed RM, Hultén MA.
    Am J Hum Genet; 2000 Sep 14; 67(3):601-9. PubMed ID: 10936106
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  • 26. Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation.
    Cetin Z, Mihci E, Keser I, Karaali K, Berker S, Luleci G.
    Genet Couns; 2012 Sep 14; 23(2):239-47. PubMed ID: 22876583
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  • 33. Meiotic chromosome segregation in human t(11;22)(q23;q11) carriers: a theoretical consideration.
    Koduru PR, Chaganti RS.
    Genome; 1989 Feb 14; 32(1):24-9. PubMed ID: 2721946
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  • 34. Partial trisomy 13q identified by sequential fluorescence in situ hybridization.
    Rao VV, Carpenter NJ, Gucsavas M, Coldwell J, Say B.
    Am J Med Genet; 1995 Jul 31; 58(1):50-3. PubMed ID: 7573156
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  • 35. Trisomy 16pter to 16q12.1 and monosomy 22pter to 22q11.2 resulting from adjacent-2 segregation of a maternal complex chromosome rearrangement.
    Xu J, Chernos J, Roland B.
    Am J Med Genet; 1997 Dec 19; 73(3):327-9. PubMed ID: 9415693
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  • 37. A family study of complex chromosome rearrangement involving chromosomes 1, 8, and 11 and its reproductive consequences.
    Trpchevska N, Dimova I, Arabadji T, Milachich T, Angelova S, Dimitrova M, Hristova-Savova M, Andreeva P, Timeva T, Shterev A.
    J Assist Reprod Genet; 2017 May 19; 34(5):659-669. PubMed ID: 28236108
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  • 39. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
    Aglan MS, Kamel AK, Helmy NA.
    Genet Couns; 2008 May 19; 19(2):199-209. PubMed ID: 18618995
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  • 40. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
    Chen CP, Chen M, Su YN, Huang JP, Ma GC, Chang SP, Chern SR, Chen YT, Su JW, Lee CC, Town DD, Wang W.
    Taiwan J Obstet Gynecol; 2012 Jun 19; 51(2):245-52. PubMed ID: 22795102
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