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Journal Abstract Search

233 related items for PubMed ID: 25119912

  • 1. [Detection of mosaic trisomy 9 missed by conventional cytogenetics using SNP-array and fluorescence in situ hybridization].
    Luo Y, Chen S, Li H, Pan L, Shen M, Jin F, Xu C.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Aug; 31(4):469-71. PubMed ID: 25119912
    [Abstract] [Full Text] [Related]

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  • 3. Resolution of trisomic mosaicism in prenatal diagnosis: estimated performance of a 50K SNP microarray.
    Cross J, Peters G, Wu Z, Brohede J, Hannan GN.
    Prenat Diagn; 2007 Dec; 27(13):1197-204. PubMed ID: 17994637
    [Abstract] [Full Text] [Related]

  • 4. Prenatal diagnosis of maternal uniparental disomy 21 in association with low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with intrauterine growth restriction and a favorable outcome.
    Chen CP, Liou JD, Chern SR, Wu PS, Chen SW, Wu FT, Lee MS, Chen YY, Wang W.
    Taiwan J Obstet Gynecol; 2022 Jan; 61(1):146-149. PubMed ID: 35181027
    [Abstract] [Full Text] [Related]

  • 5. Detection of maternal uniparental disomy 9 in association with low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with intrauterine growth restriction, abnormal first-trimester screening result (low PAPP-A and low PlGF), maternal preeclampsia and a favorable outcome.
    Chen CP, Chern SR, Wu PS, Chen SW, Wu FT, Chen LF, Chen YY, Wang W.
    Taiwan J Obstet Gynecol; 2022 Jan; 61(1):141-145. PubMed ID: 35181026
    [Abstract] [Full Text] [Related]

  • 6. Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review.
    Chen CP, Chen M, Pan YJ, Su YN, Chern SR, Tsai FJ, Chen YT, Wang W.
    Taiwan J Obstet Gynecol; 2011 Sep; 50(3):331-8. PubMed ID: 22030049
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  • 7. Partial trisomy 8 mosaicism not detected by cultured amniotic-fluid cells.
    Tsai MC, Cheng HY, Su MT, Chen M, Kuo PL.
    Taiwan J Obstet Gynecol; 2014 Dec; 53(4):598-601. PubMed ID: 25510708
    [Abstract] [Full Text] [Related]

  • 8. Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses.
    Chen CP, Lin HM, Su YN, Chern SR, Tsai FJ, Wu PC, Lee CC, Chen YT, Lee MS, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2010 Sep; 49(3):341-50. PubMed ID: 21056321
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  • 10. Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis.
    Chen CP, Su YN, Su JW, Chern SR, Chen YT, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2013 Mar; 52(1):97-105. PubMed ID: 23548227
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  • 11. Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review.
    Chen CP, Chern SR, Chen YN, Wu PS, Yang CW, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2015 Aug; 54(4):426-31. PubMed ID: 26384064
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  • 13. Trisomy 7 mosaicism prenatally misdiagnosed and maternal uniparental disomy in a child with pigmentary mosaicism and Russell- Silver syndrome.
    Petit F, Holder-Espinasse M, Duban-Bedu B, Bouquillon S, Boute-Benejean O, Bazin A, Rouland V, Manouvrier-Hanu S, Delobel B.
    Clin Genet; 2012 Mar; 81(3):265-71. PubMed ID: 21204802
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  • 14. Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism.
    Chen CP, Chen YY, Chern SR, Wu PS, Su JW, Chen YT, Lee CC, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2013 Sep; 52(3):395-400. PubMed ID: 24075380
    [Abstract] [Full Text] [Related]

  • 15. Prenatal diagnosis of a trisomy 7 mosaic case: CMA, CNV-seq, karyotyping, interphase FISH, and MS-MLPA, which technique to choose?
    Cong X, Zhang T, Li Z, Luo X, Hu L, Liu W.
    BMC Pregnancy Childbirth; 2024 May 03; 24(1):338. PubMed ID: 38702634
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  • 16. Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature review.
    Chen CP, Wang LK, Chern SR, Chen YN, Chen SW, Wu PS, Town DD, Pan CW, Yang CW, Wang W.
    Taiwan J Obstet Gynecol; 2016 Oct 03; 55(5):712-717. PubMed ID: 27751421
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  • 17. Detection of no isochromosome 20q by interphase fluorescent in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis.
    Chen CP, Su JW, Chern SR, Kuo YL, Wu PS, Lee MS, Yang CW, Wang W.
    Taiwan J Obstet Gynecol; 2015 Feb 03; 54(1):58-61. PubMed ID: 25675921
    [Abstract] [Full Text] [Related]

  • 18. Mosaic trisomy 2 at amniocentesis: prenatal diagnosis and molecular genetic analysis.
    Chen CP, Su YN, Chern SR, Chen YT, Wu PS, Su JW, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2012 Dec 03; 51(4):603-11. PubMed ID: 23276565
    [Abstract] [Full Text] [Related]

  • 19. Perinatal cytogenetic discrepancy in a fetus with low-level mosaicism for trisomy 21 and a favorable outcome.
    Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Wang W.
    Taiwan J Obstet Gynecol; 2020 May 03; 59(3):440-442. PubMed ID: 32416895
    [Abstract] [Full Text] [Related]

  • 20. Rapid diagnosis of pseudomosaicism in a case of Level II mosaicism for trisomy 5 in a single colony from an in situ culture of amniocytes and a review of mosaic trisomy 5 at amniocentesis.
    Chen CP, Chang SJ, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2016 Aug 03; 55(4):602-3. PubMed ID: 27590391
    [Abstract] [Full Text] [Related]

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