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Journal Abstract Search

807 related items for PubMed ID: 23040926

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  • 4. 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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  • 7. Prenatal diagnosis of mosaic tetrasomy 18p.
    Chen CP, Ko TM, Su YN, Chern SR, Su JW, Chen YT, Town DD, Wang W.
    Taiwan J Obstet Gynecol; 2012 Dec; 51(4):625-9. PubMed ID: 23276569
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  • 8. 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
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  • 9. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16.
    Chen CP, Ko TM, Chern SR, Wu PS, Chen SW, Lai ST, Yang CW, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2017 Aug; 56(4):545-549. PubMed ID: 28805616
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  • 10. 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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  • 12. Interphase fluorescence in situ hybridization characterization of mosaicism using uncultured amniocytes and cultured stimulated cord blood lymphocytes in prenatally detected Pallister-Killian syndrome.
    Chen CP, Peng CR, Chern SR, Kuo YL, Wu PS, Town DD, Pan CW, Yang CW, Wang W.
    Taiwan J Obstet Gynecol; 2014 Dec; 53(4):566-71. PubMed ID: 25510702
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  • 13. 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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  • 14. 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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  • 16. 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; 51(4):603-11. PubMed ID: 23276565
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  • 17. Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1-q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality.
    Chen CP, Chern SR, Chen YN, Chen SW, Wu PS, Yang CW, Lee CC, Lee MS, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2017 Apr; 56(2):217-223. PubMed ID: 28420511
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  • 18. Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9.
    Chen CP, Chen M, Wang LK, Chern SR, Wu PS, Chen SW, Lai ST, Chang SP, Yang CW, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2017 Aug; 56(4):527-533. PubMed ID: 28805612
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  • 20. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13.
    Chen CP, Tsai CH, Chern SR, Wu PS, Su JW, Lee CC, Chen YT, Chen WL, Chen LF, Wang W.
    Gene; 2013 Oct 15; 529(1):163-8. PubMed ID: 23933417
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