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146 related items for PubMed ID: 35595446

  • 1. Prenatal diagnosis and molecular cytogenetic characterization of partial dup (18p)/del (18q) due to a maternal pericentric inversion 18 in a foetus with multiple anomalies.
    Atli EI, Atli E, Inan C, Varol GF, Mail C, Erbilen EA, Yalcintepe S, Demir S, Gurkan H.
    Taiwan J Obstet Gynecol; 2022 May; 61(3):504-509. PubMed ID: 35595446
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  • 2. Prenatal diagnosis and molecular cytogenetic characterization of partial dup(18q)/del(18p) due to a paternal pericentric inversion 18 in a fetus with multiple anomalies.
    Lee MJ, Park SH, Shim SH, Moon MJ, Cha DH.
    Taiwan J Obstet Gynecol; 2019 May; 58(3):318-323. PubMed ID: 31122516
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  • 3. Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion.
    Chen CP, Ko TM, Su YN, Wang LK, Chern SR, Wu PS, Chen YN, Chen SW, Ko K, Lee CC, Chen LF, Yang CW, Wang W.
    Taiwan J Obstet Gynecol; 2016 Oct; 55(5):733-737. PubMed ID: 27751426
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  • 6. Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion.
    Chen CP, Chen CY, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Town DD, Lee MS, Yang CW, Wang W.
    Taiwan J Obstet Gynecol; 2016 Oct; 55(5):705-711. PubMed ID: 27751420
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  • 8. Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization.
    Chen CP, Ko TM, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2019 Sep; 58(5):698-703. PubMed ID: 31542096
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  • 10. Detection of a rare de novo 18p terminal deletion with inverted duplication in a Chinese pregnant woman.
    Zhu J, Qi H, Cao S, Cai L, Wen X, Tang G, Wan Q, Chen C, Wang J, Zeng W, Luo Y.
    Mol Genet Genomic Med; 2019 Sep; 7(9):e868. PubMed ID: 31317671
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  • 12. 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; 51(2):245-52. PubMed ID: 22795102
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  • 16. Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly.
    Chen CP, Kuo YK, Su YN, Chern SR, Tsai FJ, Wu PC, Chen YT, Town DD, Wang W.
    Taiwan J Obstet Gynecol; 2011 Jun; 50(2):182-7. PubMed ID: 21791305
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  • 17. Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, inv(18)(p11.2q21.3).
    Asano T, Ikeuchi T, Shinohara T, Enokido H, Hashimoto K.
    Jinrui Idengaku Zasshi; 1991 Sep; 36(3):257-65. PubMed ID: 1753439
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  • 18. Low-level complex mosaic with multiple cell lines affecting the 18q21.31q21.32 region in a patient with de novo 18q terminal deletion.
    Bonaglia MC, Fichera M, Marelli S, Romaniello R, Zuffardi O.
    Eur J Med Genet; 2022 Nov; 65(11):104596. PubMed ID: 36064004
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  • 19. Prenatal diagnosis of 18p deletion and isochromosome 18q mosaicism in a fetus with a cystic hygroma.
    Vičić A, Hafner T, Wagner J, Stipoljev F.
    Coll Antropol; 2014 Sep; 38(3):1059-62. PubMed ID: 25420396
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  • 20. Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.
    Chen CP, Su YN, Chern SR, Hsu CY, Tsai FJ, Wu PC, Lee CC, Chen YT, Lee MS, Wang W.
    Taiwan J Obstet Gynecol; 2011 Mar; 50(1):67-73. PubMed ID: 21482378
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