BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 38702634)

  • 1. 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; 24(1):338. PubMed ID: 38702634
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Use of the MS-MLPA assay in prenatal diagnosis of Prader-Willi syndrome with mosaic trisomy 15.
    Zhang M; Liang Y; Li H; Xu F
    Taiwan J Obstet Gynecol; 2024 Jan; 63(1):81-84. PubMed ID: 38216276
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 18 at amniocentesis in a pregnancy with a favorable fetal outcome and maternal uniparental disomy 18.
    Chen CP; Su JW; Chern SR; Wu PS; Chen SW; Wu FT; Chen WL; Lee MS; Pan CW; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2022 Jul; 61(4):684-689. PubMed ID: 35779922
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The significance of trisomy 7 mosaicism in noninvasive prenatal screening.
    Qi Y; Yang J; Hou Y; Guo F; Peng H; Wang D; Du Q; Yin A
    Hum Genomics; 2019 Apr; 13(1):18. PubMed ID: 30971315
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis in a pregnancy with a favorable outcome.
    Chen CP; Ko TM; Chen TC; Chern SR; Wu PS; Chen SW; Wu FT; Chen WL; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2022 Jul; 61(4):677-683. PubMed ID: 35779921
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Accidental discovery of copy number variation on chromosome 1 in a fetus with high risk of trisomy 13 suggested by NIPT].
    Chang J; Song Y; Qi Q; Hao N; Liu J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Aug; 40(8):922-927. PubMed ID: 37532489
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetus.
    Chen CP; Ko TM; Chern SR; Wu PS; Chen SW; Wu FT; Chen YY; Town DD; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2021 May; 60(3):534-539. PubMed ID: 33966743
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Low-level mosaic trisomy 15 at amniocentesis without uniparental disomy 15 in a pregnancy associated with cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes, a favorable fetal outcome and perinatal decrease of the aneuploid cell line.
    Chen CP; Chen SW; Chern SR; Wu PS; Wu FT; Pan YT; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2023 Mar; 62(2):358-362. PubMed ID: 36965910
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Low-level mosaic trisomy 9 at amniocentesis associated with a positive non-invasive prenatal testing for trisomy 9, maternal uniparental disomy 9, intrauterine growth restriction and a favorable fetal outcome in a pregnancy.
    Chen CP; Ko TM; Chen SW; Chern SR; Wu FT; Pan YT; Pan CW; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2023 May; 62(3):457-460. PubMed ID: 37188454
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Low-level mosaic trisomy 13 at amniocentesis in a pregnancy associated with a positive NIPT result suspicious of trisomy 13, a CVS result of mosaic trisomy 13, cytogenetic discrepancy in various tissues and a favorable fetal outcome.
    Chen CP; Chen M; Ma GC; Chang SP; Wu FT; Pan YT; Chern SR; Chen WL; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2023 Jul; 62(4):577-581. PubMed ID: 37407198
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of low-level mosaic trisomy 17 with maternal uniparental disomy 17 by amniocentesis in a pregnancy with a favorable outcome.
    Chen CP; Lin SY; Chern SR; Wu PS; Chen SW; Wu FT; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2020 Mar; 59(2):301-305. PubMed ID: 32127154
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Low-level mosaic trisomy 21 at amniocentesis and cordocentesis in the second trimester in a pregnancy associated with positive non-invasive prenatal testing for trisomy 21, perinatal progressive decrease of the trisomy 21 cell line and a favorable fetal outcome.
    Chen CP; Wu FT; Pan YT; Wu PS; Lee MS; Chiu CL; Wang W
    Taiwan J Obstet Gynecol; 2024 May; 63(3):391-393. PubMed ID: 38802204
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of mosaicism for double aneuploidy of 47,XXY and trisomy 7 (48,XXY,+7) at amniocentesis in a pregnancy with a favorable outcome.
    Chen CP; Tsai HT; Chern SR; Wu PS; Chen SW; Wu FT; Chen YY; Town DD; Chen WL; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2021 May; 60(3):543-548. PubMed ID: 33966745
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Karyotyping and prenatal diagnosis of 47,XX,+ 8[67]/46,XX [13] Mosaicism: case report and literature review.
    Sun S; Zhan F; Jiang J; Zhang X; Yan L; Cai W; Liu H; Cao D
    BMC Med Genomics; 2019 Dec; 12(1):197. PubMed ID: 31864361
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis.
    Chen CP; Hsu TY; Ko TM; Chern SR; Wu PS; Chen SW; Wu FT; Chen YY; Lee CC; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2020 Sep; 59(5):728-735. PubMed ID: 32917326
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.