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Journal Abstract Search

606 related items for PubMed ID: 23933417

  • 21. 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
    [Abstract] [Full Text] [Related]

  • 22. 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
    [Abstract] [Full Text] [Related]

  • 23. 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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  • 24. 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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  • 25. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities.
    Chen CP, Lin SP, Lin YH, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Chen WL, Wang W.
    Taiwan J Obstet Gynecol; 2016 Dec; 55(6):852-855. PubMed ID: 28040132
    [Abstract] [Full Text] [Related]

  • 26. 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
    [Abstract] [Full Text] [Related]

  • 27. Low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with a favorable fetal outcome, intrauterine growth restriction, cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes and perinatal progressive decrease of the aneuploid cell line.
    Chen CP, Lai TH, Chen SW, Chern SR, Wu FT, Wu PS, Pan YT, Chen WL, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2023 May; 62(3):461-465. PubMed ID: 37188455
    [Abstract] [Full Text] [Related]

  • 28. 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
    [Abstract] [Full Text] [Related]

  • 29. Mosaic distal 9p deletion or 46,XY,del(9)(p23)/46,XY at amniocentesis in a pregnancy associated with perinatal progressive decrease of the aneuploid cell line and a favorable fetal outcome.
    Chen CP, Wu FT, Pan YT, Wu PS, Lee CC, Chen WL, Chiu CL, Wang W.
    Taiwan J Obstet Gynecol; 2024 Jul; 63(4):540-544. PubMed ID: 39004483
    [Abstract] [Full Text] [Related]

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  • 33. Mosaic isochromosome 20q at amniocentesis: Prenatal diagnosis, genetic counseling and literature review.
    Chen CP, Chern SR, Wu PS, Chen SW, Wu FT, Town DD, Wang W.
    Taiwan J Obstet Gynecol; 2019 Nov; 58(6):855-858. PubMed ID: 31759542
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  • 34. Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review.
    Chen CP, Chen M, Su YN, Huang JP, Chern SR, Wu PS, Su JW, Chang SP, Chen YT, Lee CC, Chen LF, Pan CW, Wang W.
    Gene; 2013 Oct 15; 529(1):169-75. PubMed ID: 23933412
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  • 37. Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic trisomy 20 at amniocentesis in a pregnancy with a favorable outcome.
    Chen CP, Lin YH, Wu PS, Chern SR, Chen SW, Wu FT, Lee CC, Pan CW, Chen YY, Wang W.
    Taiwan J Obstet Gynecol; 2022 Jan 15; 61(1):138-140. PubMed ID: 35181025
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  • 38. Mosaic 46,XY,dup(14) (q12q22.3)/46, XY at amniocentesis in a pregnancy associated with a favorable fetal outcome and cytogenetic discrepancy in various tissues.
    Chen CP, Wu FT, Chen CY, Chen SW, Chern SR, Wu PS, Pan YT, Lee CC, Lee MS, Chen YY, Wang W.
    Taiwan J Obstet Gynecol; 2023 Mar 15; 62(2):343-347. PubMed ID: 36965906
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  • 39. Prenatal diagnosis and molecular cytogenetic characterization of a pure ring chromosome 21 with a 4.657-Mb 21q22.3 deletion.
    Chen CP, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Chen YY, Town DD, Wang W.
    Taiwan J Obstet Gynecol; 2021 Jan 15; 60(1):157-160. PubMed ID: 33494993
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