BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

233 related articles for article (PubMed ID: 33494995)

  • 1. 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]  

  • 2. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects.
    Kuo YL; Chen CP; Wang LK; Ko TM; Chang TY; Chern SR; Wu PS; Chen YT; Chang SY
    Taiwan J Obstet Gynecol; 2014 Jun; 53(2):248-51. PubMed ID: 25017279
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review.
    Chen CP; Huang JP; Chen YY; Chern SR; Wu PS; Su JW; Chen YT; Chen WL; Wang W
    Gene; 2013 Sep; 527(1):405-9. PubMed ID: 23791650
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones.
    Chen CP; Chen CY; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Yang CW; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2017 Dec; 56(6):821-826. PubMed ID: 29241927
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prenatal diagnosis of familial 2p15 microduplication associated with pulmonary artery stenosis, single umbilical artery and left foot postaxial polydactyly on fetal ultrasound.
    Chen CP; Chern SR; Wu PS; Chen SW; Wu FT; Wang W
    Taiwan J Obstet Gynecol; 2021 Jan; 60(1):161-164. PubMed ID: 33494994
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Prenatal diagnosis and perinatal findings of 17q12 microdeletion encompassing HNF1B in a fetus with bilateral hyperechogenic kidneys on fetal ultrasound and mild renal abnormality after birth, and a review of the literature of prenatal diagnosis of 17q12 microdeletion.
    Chen CP; Wu FT; Pan YT; Wu PS; Wang W
    Taiwan J Obstet Gynecol; 2024 Jan; 63(1):77-80. PubMed ID: 38216274
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal diagnosis of a 1.651-Mb 19q13.42-q13.43 microdeletion in a fetus with micrognathia and bilateral pyelectasis on prenatal ultrasound.
    Chen CP; Hsu CY; Chern SR; Wu PS; Chen SW; Wu FT; Wang W
    Taiwan J Obstet Gynecol; 2020 Sep; 59(5):763-765. PubMed ID: 32917333
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicystic kidney, and variable clinical spectrum in the family.
    Chen CP; Chang SD; Wang TH; Wang LK; Tsai JD; Liu YP; Chern SR; Wu PS; Su JW; Chen YT; Wang W
    Taiwan J Obstet Gynecol; 2013 Dec; 52(4):551-7. PubMed ID: 24411042
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion.
    Chen YN; Chen CP; Ko TM; Wang LK; Wu PC; Chang TY; Wu PS; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2016 Feb; 55(1):117-20. PubMed ID: 26927262
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability.
    Chen CP; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Chen WL; Yang CW; Wang W
    Taiwan J Obstet Gynecol; 2018 Aug; 57(4):578-582. PubMed ID: 30122582
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound.
    Chen CP; Chang SY; Chen YN; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Yang CW; Chen LF; Wang W
    Taiwan J Obstet Gynecol; 2018 Oct; 57(5):739-744. PubMed ID: 30342663
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. [Congenital cardiovascular malformations and chromosome microdeletions in 22q11.2].
    Trost D; Engels H; Bauriedel G; Wiebe W; Schwanitz G
    Dtsch Med Wochenschr; 1999 Jan; 124(1-2):3-7. PubMed ID: 9951451
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.