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Journal Abstract Search

214 related items for PubMed ID: 28040139

  • 1. Prenatal diagnosis of paternal duplication of 11p15.5→14.3: Its implication of Beckwith-Wiedemann syndrome.
    Chen KJ, Liu YM, Li CH, Chang YL, Chang SD.
    Taiwan J Obstet Gynecol; 2016 Dec; 55(6):877-880. PubMed ID: 28040139
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  • 2. Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer.
    Chen CP, Su YN, Chen SU, Chang TY, Wu PC, Chern SR, Wu PS, Kuo YL, Wang W.
    Taiwan J Obstet Gynecol; 2014 Mar; 53(1):90-4. PubMed ID: 24767654
    [Abstract] [Full Text] [Related]

  • 3. Detection of hypermethylation at H19DMR at amniocentesis in a fetus with overgrowth, distended abdomen and Beckwith-Wiedemann syndrome.
    Chen CP, Chern SR, Lin CH, Hsu CY, Lin HY, Wu FT, Chen SW, Wang W.
    Taiwan J Obstet Gynecol; 2021 Nov; 60(6):1103-1106. PubMed ID: 34794746
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  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Pure partial monosomy 3p (3p25.3 → pter): prenatal diagnosis and array comparative genomic hybridization characterization.
    Chen CP, Su YN, Chen CY, Su JW, Chern SR, Town DD, Wang W.
    Taiwan J Obstet Gynecol; 2012 Sep; 51(3):435-9. PubMed ID: 23040932
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  • 6. Paternal origin of 11p15 duplications in the Beckwith-Wiedemann syndrome. A new case and review of the literature.
    Brown KW, Gardner A, Williams JC, Mott MG, McDermott A, Maitland NJ.
    Cancer Genet Cytogenet; 1992 Jan; 58(1):66-70. PubMed ID: 1728953
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  • 8. Molecular and genomic characterisation of cryptic chromosomal alterations leading to paternal duplication of the 11p15.5 Beckwith-Wiedemann region.
    Russo S, Finelli P, Recalcati MP, Ferraiuolo S, Cogliati F, Dalla Bernardina B, Tibiletti MG, Agosti M, Sala M, Bonati MT, Larizza L.
    J Med Genet; 2006 Aug; 43(8):e39. PubMed ID: 16882733
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  • 9. Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia.
    Chen CP, Wang YL, Chern SR, Liu YP, Peng CR, Kuo YL, Wu PS, Chen WL, Wang W.
    Taiwan J Obstet Gynecol; 2015 Feb; 54(1):66-70. PubMed ID: 25675923
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  • 12. 11p15 duplication and 13q34 deletion with Beckwith-Wiedemann syndrome and factor VII deficiency.
    Jurkiewicz D, Kugaudo M, Tańska A, Wawrzkiewicz-Witkowska A, Tomaszewska A, Kucharczyk M, Cieślikowska A, Ciara E, Krajewska-Walasek M.
    Pediatr Int; 2015 Jun; 57(3):486-91. PubMed ID: 26012727
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  • 14. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8.
    Chen CP, Chen M, Ko TM, Ma GC, Tsai FJ, Tsai MS, Wu PC, Lee CC, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2010 Dec; 49(4):500-5. PubMed ID: 21199754
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  • 15. 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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  • 16. Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase fluorescence in situ hybridization, quantitative fluorescent polymerase chain reaction, and array comparative genomic hybridization on uncultured amniocytes in a pregnancy with fetal pyelectasis.
    Chen CP, Chang SD, Su YN, Chen M, Chern SR, Su JW, Chen YT, Chen WL, Pan CW, Lee MS, Wang W.
    Taiwan J Obstet Gynecol; 2012 Sep; 51(3):405-10. PubMed ID: 23040926
    [Abstract] [Full Text] [Related]

  • 17. Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome.
    Slavotinek A, Gaunt L, Donnai D.
    J Med Genet; 1997 Oct; 34(10):819-26. PubMed ID: 9350814
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  • 18. Unusual prenatal presentation of Beckwith-Wiedemann syndrome.
    Mulik V, Wellesley D, Sawdy R, Howe DT.
    Prenat Diagn; 2004 Jul; 24(7):501-3. PubMed ID: 15300738
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  • 19. Wiedemann-Beckwith syndrome and chromosomal duplication 4q/deficiency 18p.
    Fryns JP, Kleczkowska A, Devriendt K, Devliegher H, Van den Berghe H.
    Genet Couns; 1993 Jul; 4(1):37-41. PubMed ID: 8471219
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  • 20. Beckwith-Wiedemann syndrome: difficulties with prenatal diagnosis.
    Nowotny T, Bollmann R, Pfeifer L, Windt E.
    Fetal Diagn Ther; 1994 Jul; 9(4):256-60. PubMed ID: 7945907
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