BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

245 related articles for article (PubMed ID: 29241933)

  • 21. 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]  

  • 22. Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1.
    Chen CP; Lin MH; Chen YY; Chern SR; Chen YN; Wu PS; Pan CW; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2015 Oct; 54(5):592-6. PubMed ID: 26522117
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 1q42.3-q44 deletion in a fetus associated with ventriculomegaly on prenatal ultrasound.
    Chen CP; Ko TM; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen YY; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2020 Jul; 59(4):598-603. PubMed ID: 32653137
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound.
    Chen CP; Chang TY; Hung FY; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2017 Dec; 56(6):843-846. PubMed ID: 29241932
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mosaic tetrasomy 9p at amniocentesis in a pregnancy associated with a favorable fetal outcome, perinatal progressive decrease of the aneuploid cell line and cytogenetic discrepancy in various tissues.
    Chen CP; Chen SW; Chern SR; Wu PS; Wu FT; Pan YT; Lee CC; Pan CW; Chen YY; Wang W
    Taiwan J Obstet Gynecol; 2023 Jan; 62(1):148-154. PubMed ID: 36720529
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Molecular cytogenetic characterization of de novo concomitant proximal 21q deletion of 21q11.2q21.3 and distal Xp deletion of Xp22.33p22.2 due to an unbalanced X;21 translocation detected by amniocentesis.
    Chen CP; Chen SW; Wu CY; Chern SR; Wu FT; Pan YT; Wu PS; Lee CC; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2023 Jan; 62(1):123-127. PubMed ID: 36720524
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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
    [TBL] [Abstract][Full Text] [Related]  

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

  • 29. Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 20p (20p12-p13) encompassing JAG1 and a literature review of prenatal diagnosis of Alagille syndrome.
    Chen CP; Yin CS; Wang LK; Chern SR; Chen SW; Lai ST; Wu PS; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2017 Jun; 56(3):390-393. PubMed ID: 28600057
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase fluorescence in situ hybridization, quantitative fluorescent polymerase chain reaction, and array comparative genomic hybridization on uncultured amniocytes in a pregnancy with fetal pyelectasis.
    Chen CP; Chang SD; Su YN; Chen M; Chern SR; Su JW; Chen YT; Chen WL; Pan CW; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2012 Sep; 51(3):405-10. PubMed ID: 23040926
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.
    Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Wu PC; Chen WL; Chen LF; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2011 Jun; 50(2):188-95. PubMed ID: 21791306
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prenatal diagnosis and molecular cytogenetic characterization of a de novo duplication of 2q12.2→q13 encompassing MALL, NPHP1, RGPD6 and BUB1.
    Chen CP; Chen SW; Chern SR; Wu PS; Wu FT; Pan YT; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2022 Nov; 61(6):1044-1047. PubMed ID: 36427971
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy.
    Chen CP; Su YN; Hsu CY; Chern SR; Lee CC; Chen YT; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2011 Dec; 50(4):485-91. PubMed ID: 22212322
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Prenatal diagnosis and molecular cytogenetic characterization of a de novo proximal interstitial deletion of chromosome 4p (4p15.2→p14).
    Chen CP; Lee MJ; Chern SR; Wu PS; Su JW; Chen YT; Lee MS; Wang W
    Gene; 2013 Oct; 529(2):351-6. PubMed ID: 23948085
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interchromosomal insertion of ins(1;8)(p22.1;q22q23).
    Chen CP; Wu CY; Chern SR; Wu PS; Chen SW; Wu FT; Chen YY; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2020 May; 59(3):437-439. PubMed ID: 32416894
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency.
    Chen CP; Lin CJ; Chen YN; Chern SR; Chen SW; Lai ST; Wu PS; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2017 Jun; 56(3):398-401. PubMed ID: 28600059
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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; 529(1):163-8. PubMed ID: 23933417
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results.
    Chen CP; Liou JD; Seow KM; Chern SR; Wu PS; Chen SW; Wu FT; Town DD; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2020 Sep; 59(5):758-762. PubMed ID: 32917332
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from 2q11.1-q12.1 associated with fetal bilateral radial dysplasia.
    Chen CP; Lin CJ; Chen SW; Wu FT; Chern SR; Wu PS; Chen YY; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2020 Nov; 59(6):941-944. PubMed ID: 33218417
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.