These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

209 related articles for article (PubMed ID: 14755410)

  • 21. 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; 61(1):138-140. PubMed ID: 35181025
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. 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]  

  • 24. Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome.
    Chen CP; Ko TM; Chen YY; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Yang CW; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2017 Dec; 56(6):836-839. PubMed ID: 29241930
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mosaic trisomy 22 at amniocentesis: Prenatal diagnosis and literature review.
    Chen CP; Huang MC; Chern SR; Wu PS; Chen SW; Chuang TY; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2019 Sep; 58(5):692-697. PubMed ID: 31542095
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prenatal diagnosis of trisomy 11 in a single colony of cultured amniocytes at amniocentesis in a pregnancy with a favorable outcome.
    Chen CP; Hsieh CE; Chern SR; Chen SW; Wu FT; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2021 May; 60(3):540-542. PubMed ID: 33966744
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prenatal diagnosis of low-level mosaicism for a small supernumerary marker chromosome derived from chromosome 9q (9q13-q21.33) in a pregnancy with a favorable outcome, and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes.
    Chen CP; Lo LM; Ko TM; Chern SR; Wu PS; Chen SW; Wu FT; Town DD; Chen LF; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2021 Mar; 60(2):331-334. PubMed ID: 33678337
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mosaic trisomy 18 at amniocentesis associated with a favorable fetal outcome in a pregnancy.
    Chen CP; Hsu TY; Tsai CC; Chern SR; Chen SW; Wu FT; Wu PS; Lee CC; Chen LF; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2022 Jul; 61(4):690-694. PubMed ID: 35779923
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Progressive increase of the mosaic level for 45,X in 45,X/46, XX at different amniocenteses and postnatal progressive decrease of the 45,X cell line in a mosaic 45,X/46, XX fetus with a favorable outcome.
    Chen CP; Chern SR; Chen SW; Wu FT; Lee CC; Chen WL; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2022 Sep; 61(5):876-879. PubMed ID: 36088060
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Wolf-Hirschhorn syndrome: Prenatal diagnosis and molecular cytogenetic characterization of a de novo distal deletion of 4p (4p16.1 → pter) in a fetus with facial cleft and preaxial polydactyly.
    Chen CP; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen LF; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2020 May; 59(3):425-431. PubMed ID: 32416892
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Prenatal diagnosis of premature centromere division-related mosaic variegated aneuploidy.
    Chen CP; Lee CC; Chen WL; Wang W; Tzen CY
    Prenat Diagn; 2004 Jan; 24(1):19-25. PubMed ID: 14755404
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mosaic trisomy 21 at amniocentesis associated with a favorable fetal outcome and perinatal progressive decrease of the trisomy 21 cell line.
    Chen CP; Chen SW; Wang LK; Chern SR; Wu PS; Wu FT; Pan YT; Lee CC; Chen LF; Pan CW; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2023 Jan; 62(1):132-136. PubMed ID: 36720526
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.
    Chen CP; Chen M; Chern SR; Wu PS; Chang SP; Lee DJ; Chen YT; Chen LF; Su JW; Hwa-Ruey Hsieh A; Hwa-Jiun Hsieh A; Wang W
    Taiwan J Obstet Gynecol; 2012 Sep; 51(3):411-7. PubMed ID: 23040927
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome.
    Chen CP; Lin CJ; Chern SR; Wu PS; Chen YN; Chen SW; Pan CW; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2017 Apr; 56(2):238-242. PubMed ID: 28420516
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 21 associated with low PAPP-A and low PlGF in the first-trimester maternal serum screening.
    Chen CP; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Lee CC; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2022 Mar; 61(2):359-363. PubMed ID: 35361402
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Low-level mosaic trisomy 17 at amniocentesis in a pregnancy associated with a favorable fetal outcome and cytogenetic discrepancy between cultured and uncultured amniocytes.
    Chen CP; Chen SW; Chern SR; Chen YY; Wu FT; Pan YT; Lee CC; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2023 Mar; 62(2):351-353. PubMed ID: 36965908
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
    Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
    Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion.
    Chen CP; Ko TM; Su YN; Wang LK; Chern SR; Wu PS; Chen YN; Chen SW; Ko K; Lee CC; Chen LF; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Oct; 55(5):733-737. PubMed ID: 27751426
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Low-level mosaicism for trisomy 16 at amniocentesis in a pregnancy associated with intrauterine growth restriction and a favorable outcome.
    Chen CP; Chen M; Wang LK; Chern SR; Wu PS; Ma GC; Chang SP; Chen SW; Wu FT; Lee CC; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2021 Mar; 60(2):345-349. PubMed ID: 33678340
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.