BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 31400135)

  • 21. Prenatal diagnosis of a fetus with a de novo trisomy 12p by array-comparative genomic hybridization (array-CGH).
    Hung CC; Lin CH; Lin SY; Shin JC; Lee CN; Su YN
    Gene; 2012 Mar; 495(2):178-82. PubMed ID: 22248625
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Karyotype analysis of amniotic fluid cells and comparison of chromosomal abnormality rate during second trimester].
    Zhang YP; Wu JP; Li XT; Lei CX; Xu JZ; Yin M
    Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):644-8. PubMed ID: 22176986
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Two cases of partial trisomy 8p derived from paternal reciprocal translocation or maternal insertion translocation: clinical features and genetic abnormalities].
    Xiao B; Zhang JM; Ji X; Jiang WT; Hu J; Tao J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Jun; 28(3):247-50. PubMed ID: 21644216
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization.
    Chen CP; Su YN; Tsai FJ; Lin MH; Wu PC; Chern SR; Lee CC; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2011 Jun; 50(2):205-11. PubMed ID: 21791309
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Prenatal diagnosis of a fetus with trisomies of 11q23.3q25 and 22q11.1q11.21].
    Li F; Tang J; Xie X; Tang S; Wu A; Tang Q; Tan W; Guo X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Jun; 36(6):632-635. PubMed ID: 31055824
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Prenatal identification of partial 3q duplication syndrome.
    Pasińska M; Adamczak R; Repczyńska A; Łazarczyk E; Iskra B; Runge AK; Haus O
    BMC Med Genomics; 2019 Jun; 12(1):85. PubMed ID: 31196198
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Prenatal genetic analysis of a fetus with Wolf-Hirschhorn syndrome and Edward syndrome].
    Shen X; He P; Fang R; Yao J; Li W
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct; 34(5):714-717. PubMed ID: 28981940
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Prenatal diagnosis of partial trisomy 3q (3q27.3→qter) and partial monosomy 14q (14q31.3→qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints.
    Chen CP; Chang YL; Chern SR; Wu PS; Su JW; Chen WL; Chen LF; Wang W
    Gene; 2013 Mar; 516(1):132-7. PubMed ID: 23266805
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Inherited unbalanced reciprocal translocation with 3q duplication and 5p deletion in a foetus revealed by cell-free foetal DNA (cffDNA) testing: a case report.
    Ali TM; Mateu-Brull E; Balaguer N; Dantas C; Borges HR; de Oliveira MQG; Rodrigo L; Campos-Galindo I; Navarro R; Milán M
    Eur J Med Res; 2021 Jun; 26(1):64. PubMed ID: 34187576
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. 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]  

  • 32. [Application of array comparative genomic hybridization in prenatal diagnosis of a case with 5q35 deletion syndrome].
    Feng Z; Hu H; Mao C; Wang D; Liu L; Liu S; Jing Z; Liu H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr; 34(2):240-243. PubMed ID: 28397228
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [A case with partial trisomy 7 (q34→qter) derived from a paternal reciprocal translocation t(7;14)(q34;q32)].
    Xiao B; Ji X; Jiang WT; Zhang JM; Hu Q; Tao J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):654-7. PubMed ID: 22161098
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Prenatal diagnosis of a fetus with 1p36 deletion syndrome and 3p26.3p25.2 duplication].
    Zhao J; Gao J; Zhao X; Li L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 May; 41(5):617-621. PubMed ID: 38684312
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Prenatal diagnosis of a rare case with de novo partial 21q(21q22.1→ qter) trisomy syndrome and absent nasal bone].
    Chen J; Sheng N; Cai M; Ge Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Aug; 38(8):783-786. PubMed ID: 34365625
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prenatal foetal diagnosis of partial trisomy 3q and monosomy 13p due to a maternal balanced rearrangement.
    Pires A; Ramos L; Venâncio M; Rei AI; Castedo S; Saraiva J
    Prenat Diagn; 2005 Apr; 25(4):292-5. PubMed ID: 15849779
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization.
    DuPont BR; Huff RW; Ridgway LE; Stratton RF; Moore CM
    Am J Med Genet; 1994 Mar; 50(1):21-7. PubMed ID: 8160748
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism.
    Chen CP; Tsai C; Lin MH; Chern SR; Chen SW; Lai ST; Chen WL; Pan CW; Wang W
    Taiwan J Obstet Gynecol; 2017 Oct; 56(5):691-693. PubMed ID: 29037560
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibs.
    Wieczorek D; Engels H; Viersbach R; Henke B; Schwanitz G; Passarge E
    J Med Genet; 1998 Jul; 35(7):545-53. PubMed ID: 9678698
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.