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 *

374 related articles for article (PubMed ID: 28600057)

  • 1. 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]  

  • 2. 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]  

  • 3. Prenatal diagnosis and molecular cytogenetic characterization of a de novo 3.19-Mb chromosome 14q32.13-q32.2 deletion of paternal origin.
    Chen CP; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen YY; Chen WL; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2020 Sep; 59(5):766-769. PubMed ID: 32917334
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
    Chen CP; Chen M; Su YN; Hsu CY; Tsai FJ; Chern SR; Wu PC; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2010 Dec; 49(4):473-80. PubMed ID: 21199750
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Pure partial monosomy 3p (3p25.3 → pter): prenatal diagnosis and array comparative genomic hybridization characterization.
    Chen CP; Su YN; Chen CY; Su JW; Chern SR; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2012 Sep; 51(3):435-9. PubMed ID: 23040932
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion.
    Chen CP; Su YN; Chen YY; Su JW; Chern SR; Chen YT; Chen WL; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2011 Dec; 50(4):506-11. PubMed ID: 22212326
    [TBL] [Abstract][Full Text] [Related]  

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

  • 9. Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1.
    Chen CP; Hsieh CH; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Yang CW; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2017 Dec; 56(6):847-851. PubMed ID: 29241933
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 15q24 microdeletion.
    Chen CP; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen YY; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2020 May; 59(3):432-436. PubMed ID: 32416893
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A 8.26Mb deletion in 6q16 and a 4.95Mb deletion in 20p12 including JAG1 and BMP2 in a patient with Alagille syndrome and Wolff-Parkinson-White syndrome.
    Le Gloan L; Pichon O; Isidor B; Boceno M; Rival JM; David A; Le Caignec C
    Eur J Med Genet; 2008; 51(6):651-7. PubMed ID: 18775522
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
    Chen CP; Huang HK; Ling PY; Su YN; Chen M; Tsai FJ; Wu PC; Chern SR; Chen YT; Lee CC; Wang W
    Taiwan J Obstet Gynecol; 2011 Dec; 50(4):492-8. PubMed ID: 22212323
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis and molecular cytogenetic characterization of de novo distal 5p deletion and distal 22q duplication.
    Chen CP; Huang JP; Chern SR; Wu PS; Chen SW; Wu FT; Chen WL; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2020 Jan; 59(1):140-145. PubMed ID: 32039783
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of the distal 11q deletion and review of the literature.
    Chen CP; Chern SR; Chang TY; Tzen CY; Lee CC; Chen WL; Chen LF; Wang W
    Prenat Diagn; 2004 Feb; 24(2):130-6. PubMed ID: 14974122
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis and molecular cytogenetic characterization of a de novo deletion of 4q34.1→qter associated with low PAPP-A and low PlGF in the first-trimester maternal serum screening, congenital heart defect on fetal ultrasound and a false negative non-invasive prenatal testing (NIPT) result.
    Chen CP; Chen SW; Wang LK; Chern SR; Wu PS; Wu FT; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2022 Nov; 61(6):1039-1043. PubMed ID: 36427970
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Alagille syndrome with deletion 20p12.2-p12.3 and hypoplastic left heart.
    Robert ML; Lopez T; Crolla J; Huang S; Owen C; Burvill-Holmes L; Stumper O; Turnpenny PD
    Clin Dysmorphol; 2007 Oct; 16(4):241-6. PubMed ID: 17786115
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot.
    Chen CP; Chen CY; Chern SR; Wu PS; Chen YN; Chen SW; Chen LF; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Apr; 55(2):270-4. PubMed ID: 27125413
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

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

    [Next]    [New Search]
    of 19.