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 *

188 related articles for article (PubMed ID: 31030440)

  • 21. [Result of prenatal diagnosis for 151 high-risk women by noninvasive prenatal screening based on high-throughput sequencing].
    Jia Y; Zhang Y; Hao W; Shi D; Meng J; Zhao H; Lian Y; Xie L; Wang X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct; 34(5):759-763. PubMed ID: 28981949
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Non-invasive prenatal testing and genetic analysis of a fetus with partial trisomy 21].
    Ma N; Liu J; Hu J; Peng Y; Xi H; Jia Z; Hu R; Wang H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Oct; 37(10):1079-1083. PubMed ID: 32924105
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Detection of copy number variants with chromosomal microarray in 10 377 pregnancies at a single laboratory.
    Lin YH; Jong YJ; Huang PC; Tsai C
    Acta Obstet Gynecol Scand; 2020 Jun; 99(6):775-782. PubMed ID: 32346853
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Identification of a fetus with complex chromosomal structural aberration by next-generation sequencing and karyotype analysis].
    Wang Y; Bai Z
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Feb; 38(2):134-137. PubMed ID: 33565065
    [TBL] [Abstract][Full Text] [Related]  

  • 25. SNP-Based Chromosomal Microarray Analysis for Detecting DNA Copy Number Variations in Fetuses with a Thickened Nuchal Fold.
    Kievskaya JK; Shilova NV; Kanivets IV; Kudryavtseva EV; Pyankov DV; Korostelev SA
    Sovrem Tekhnologii Med; 2021; 13(6):72-76. PubMed ID: 35265361
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Analysis of four fetuses with de novo chromosomal rearrangments using single nucleotide polymorphism microarray chips].
    Wang H; Xi H; Jia ZJ; Huang DM; Zhou YC; Wu LQ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Dec; 29(6):658-61. PubMed ID: 23225044
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Genetic analysis of a fetus with Pitt-Hopkins syndrome due to a 18q21.2q21.31 microdeletion].
    Zhang Y; Zeng L; Lin L; Dong X; Lin K; Chen H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 May; 41(5):622-625. PubMed ID: 38684313
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Confirmation of a maternal cryptal balanced translocation through analysis of a fetus using microarray].
    Wu J; Xie Y; Lin S; Chen B; Chen J; Zhang Z; Ji Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Feb; 32(1):69-72. PubMed ID: 25636103
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Discordant circulating fetal DNA and subsequent cytogenetics reveal false negative, placental mosaic, and fetal mosaic cfDNA genotypes.
    Lebo RV; Novak RW; Wolfe K; Michelson M; Robinson H; Mancuso MS
    J Transl Med; 2015 Aug; 13():260. PubMed ID: 26260800
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Diagnosis of a fetus with a de novo 16q partial trisomy syndrome].
    Hu L; Wang W; Li H; Zhou S; Liu S; Yang M; Bu X; He J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Oct; 37(10):1084-1086. PubMed ID: 32924106
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Genetic analysis of a fetus with partial 1q monosomy and partial 17q trisomy].
    Lin S; Zhang Z; Wu J; Ji Y; Fang Q; Chen B; Zhou Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Jun; 33(3):340-3. PubMed ID: 27264817
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Chromosome microarray analysis of four fetuses with abnormal karyotypes].
    Zhu R; Zhu X; Yang Y; Wu X; Zhang Y; Shi Y; He L; Li J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Dec; 34(6):812-815. PubMed ID: 29188606
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Application of whole-genome and high-resolution chromosome microarray analysis for the investigation of fetuses with ultrasound abnormalities].
    Zhang Y; Fu F; Li R; Xie G; Han J; Pan M; Zhen L; Yang X; Li D; Liao C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Apr; 32(2):169-74. PubMed ID: 25863078
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Reflection of a case misdiagnosed as trisomy 21 syndrome by G-banded chromosomal karyotyping analysis].
    Pei X; Liu M; Liu Y; Yang Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Oct; 36(10):1031-1034. PubMed ID: 31598954
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [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]  

  • 36. [Prenatal diagnosis of 1p36.3 microdeletion in a fetus with complex heart defect].
    Wu J; He Z; Lin S; Xie Y; Chen B; Chen J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Jun; 33(3):353-6. PubMed ID: 27264820
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Prenatal diagnosis of three fetuses with small supernumerary marker chromosomes].
    Li W; Fang R; Shen X; Yao J; Xue J; Shen G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Dec; 37(12):1344-1348. PubMed ID: 33306818
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Prenatal diagnosis of maternal partial trisomy 9p23p24.3 and 14q11.2q21.3 in a fetus: a case report.
    Wu JB; Sha J; Zhai JF; Liu Y; Zhang B
    Mol Cytogenet; 2020; 13():6. PubMed ID: 32055256
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Microarray comparative genomic hybridization (CGH)-based prenatal diagnosis for chromosome abnormalities using cell-free fetal DNA in amniotic fluid.
    Miura S; Miura K; Masuzaki H; Miyake N; Yoshiura KI; Sosonkina N; Harada N; Shimokawa O; Nakayama D; Yoshimura S; Matsumoto N; Niikawa N; Ishimaru T
    J Hum Genet; 2006; 51(5):412-417. PubMed ID: 16622586
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Prenatal diagnosis of a fetus with partial trisomy 8p resulting from a balanced maternal translocation by array-based comparative genomic hybridization].
    Guo C; Wang J; Zhao L; Liu J; Wang J; Xiao J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):375-7. PubMed ID: 26037354
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.