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 *

246 related articles for article (PubMed ID: 32039782)

  • 1. Prenatal diagnosis of concomitant distal 5q duplication and terminal 10q deletion in a fetus with intrauterine growth restriction, congenital diaphragmatic hernia and congenital heart defects.
    Chen CP; Huang JP; Chen SW; Chern SR; Wu PS; Wu FT; Chen WL; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2020 Jan; 59(1):135-139. PubMed ID: 32039782
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular cytogenetic characterization of del(X)(p22.33)mat and de novo dup(4)(q34.3q35.2) in a male fetus with multiple anomalies of facial dysmorphism, ventriculomegaly, congenital heart defects, short long bones and clinodactyly.
    Chen CP; Huang JP; Chen YY; Chen SW; Chern SR; Wu PS; Wu FT; Pan YT; Chen WL; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2023 May; 62(3):453-456. PubMed ID: 37188453
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia.
    Chen CP; Wang YL; Chern SR; Liu YP; Peng CR; Kuo YL; Wu PS; Chen WL; Wang W
    Taiwan J Obstet Gynecol; 2015 Feb; 54(1):66-70. PubMed ID: 25675923
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis.
    Chen CP; Chen CY; Chern SR; Wu PS; Chen SW; Lee CC; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2020 Jan; 59(1):130-134. PubMed ID: 32039781
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Rapid aneuploidy diagnosis of partial trisomy 7q (7q34→qter) and partial monosomy 10q (10q26.12→qter) by array comparative genomic hybridization using uncultured amniocytes.
    Chen CP; Lin SP; Su YN; Tsai FJ; Wu PC; Town DD; Chen LF; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2012 Mar; 51(1):93-9. PubMed ID: 22482977
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. High-level mosaic trisomy 14 at amniocentesis in a pregnancy associated with congenital heart defects and intrauterine growth restriction on fetal ultrasound.
    Chen CP; Wu FT; Wang LK; Pan YT; Lee MS; Wang W
    Taiwan J Obstet Gynecol; 2023 Jul; 62(4):594-596. PubMed ID: 37407202
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound.
    Chen CP; Chang SY; Wang LK; Chang TY; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Yang CW; Town DD; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2018 Oct; 57(5):730-733. PubMed ID: 30342661
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Detection of a familial 21q22.3 microduplication in a fetus associated with congenital heart defects.
    Chen CP; Chen CY; Chern SR; Wu PS; Chen SW; Chuang TY; Wang W
    Taiwan J Obstet Gynecol; 2019 Nov; 58(6):869-871. PubMed ID: 31759545
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother.
    Chen CP; Chen CY; Chern SR; Wu PS; Chen SW; Wu FT; Wang W
    Taiwan J Obstet Gynecol; 2021 Jan; 60(1):165-168. PubMed ID: 33494995
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
    Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W
    Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound.
    Chen CP; Chang SY; Lin CJ; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Chen WL; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2018 Oct; 57(5):734-738. PubMed ID: 30342662
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.