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Journal Abstract Search

345 related items for PubMed ID: 32917332

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  • 2. Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result.
    Chen CP, Ko TM, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Chen LF, Wang W.
    Taiwan J Obstet Gynecol; 2021 Jul; 60(4):775-777. PubMed ID: 34247824
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  • 4. Prenatal diagnosis of maternal uniparental disomy 5 by amniocentesis associated with confined placental mosaicism for trisomy 5 and fetal trisomy 21 in a pregnancy.
    Chen CP, Chern SR, Wang LK, Wu PS, Wu FT, Chen YY, Town DD, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2020 Nov; 59(6):938-940. PubMed ID: 33218416
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  • 6. Low-level mosaic trisomy 2 at amniocentesis in a pregnancy associated with positive NIPT and CVS results for trisomy 2, maternal uniparental disomy 2, perinatal progressive decrease of the aneuploid cell line, cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, intrauterine growth restriction and a favorable fetal outcome.
    Chen CP, Wu FT, Chern SR, Wu PS, Pan YT, Lee CC, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2023 Jul; 62(4):571-576. PubMed ID: 37407197
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  • 10. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter).
    Chen CP, Hung FY, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Wang W.
    Taiwan J Obstet Gynecol; 2016 Apr; 55(2):288-92. PubMed ID: 27125417
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  • 11. Prenatal diagnosis of mosaic trisomy 18 and maternal uniparental disomy 18 by amniocentesis in a pregnancy associated with cytogenetic discrepancy in various tissues and a favorable fetal outcome.
    Chen CP, Wu FT, Pan YT, Chern SR, Wu PS, Chiu CL, Lee CC, Chen WL, Wang W.
    Taiwan J Obstet Gynecol; 2023 Jul; 62(4):606-610. PubMed ID: 37407205
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  • 12. Prenatal diagnosis of Cri-du-Chat syndrome with concomitant distal trisomy 10q syndrome in one fetus with ultrasound anomalies.
    He JP, Qian Y, Liu WJ, Tang J, Qin MH, Luo SJ, Hou JH, Lv MX.
    Taiwan J Obstet Gynecol; 2021 Mar; 60(2):318-323. PubMed ID: 33678334
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  • 13. Prenatal diagnosis of mosaic trisomy 16 by amniocentesis in a pregnancy associated with abnormal first-trimester screening result (low PAPP-A and low PlGF), intrauterine growth restriction and a favorable outcome.
    Chen CP, Lan FH, Chern SR, Wu PS, Chen SW, Wu FT, Lee CC, Lee MS, Pan CW, Chen YY, Wang W.
    Taiwan J Obstet Gynecol; 2021 Nov; 60(6):1107-1111. PubMed ID: 34794747
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  • 20. 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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