BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 37994128)

  • 1. [Prenatal diagnosis and genetic analysis of three fetuses with duodenal atresia or stenosis].
    Chen N; Zeng W; Gao X; Luo Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Dec; 40(12):1484-1488. PubMed ID: 37994128
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal detection of chromosomal abnormalities and copy number variants in fetuses with congenital gastrointestinal obstruction.
    Meng X; Jiang L
    BMC Pregnancy Childbirth; 2022 Jan; 22(1):50. PubMed ID: 35045821
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Application of single nucleotide polymorphism array in prenatal diagnosis for fetuses with abnormal ultrasound findings].
    Guo YL; Wang L; Xue SW; Qu SZ; Yang J; Xu H; Bai ZX; Liu N; Kong XD
    Zhonghua Fu Chan Ke Za Zhi; 2018 Jul; 53(7):464-470. PubMed ID: 30078256
    [No Abstract]   [Full Text] [Related]  

  • 4. [Application of single nucleotide polymorphism array for the identification of pathogenic copy number variations in fetuses with malformations and women with an adverse reproductive history].
    Liu J; Xi H; Wang H; Jia Z; Zhou Y; Wu L
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr; 34(2):173-177. PubMed ID: 28397212
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Prenatal diagnosis and genetic analysis of two fetuses with paternally derived 17q12 microdeletions].
    Zhang Y; Liu Y; Yan L; Zhuang D; Li H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Mar; 38(3):224-227. PubMed ID: 33751529
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Value of chromosomal microarray analysis for fetuses with duodenal obstruction].
    Zhang W; Du K; Fu F; Li R; Zhang Y; Jing X; Yang X; Pan M; Zhen L; Han J; Liao C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Mar; 38(3):210-213. PubMed ID: 33751526
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal ultrasound features and genetic analysis for 17q12 microdeletion syndrome.
    Zhang Z; Pan L; Chen K; Tan R
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2021 Dec; 46(12):1370-1374. PubMed ID: 35232906
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evaluation of chromosomal abnormalities and copy number variations in fetuses with ultrasonic soft markers.
    Cai M; Lin N; Chen X; Fu M; Guo N; Xu L; Huang H
    BMC Med Genomics; 2021 Jan; 14(1):19. PubMed ID: 33435955
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical application of chromosomal microarray analysis in fetuses with increased nuchal translucency and normal karyotype.
    Su L; Huang H; An G; Cai M; Wu X; Li Y; Xie X; Lin Y; Wang M; Xu L
    Mol Genet Genomic Med; 2019 Aug; 7(8):e811. PubMed ID: 31209990
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Prenatal diagnosis of two fetuses with Xp22.31 microdeletion syndrome indicated by non-invasive prenatal testing].
    Wang R; Xi M; Wei Y; Wei L; Zhu W; Liu Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Aug; 40(8):928-932. PubMed ID: 37532490
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Prenatal detection of chromosomal abnormalities and copy number variants in fetuses with ventriculomegaly.
    Chang Q; Yang Y; Peng Y; Liu S; Li L; Deng X; Yang M; Lan Y
    Eur J Paediatr Neurol; 2020 Mar; 25():106-112. PubMed ID: 32014392
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of genetic aberrations in fetuses with pulmonary stenosis in southern China: a retrospective analysis.
    Cai M; Guo N; Fu M; Chen Y; Liang B; Que Y; Ji Q; Huang H; Xu L; Lin N
    BMC Med Genomics; 2023 May; 16(1):119. PubMed ID: 37248535
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Array-based molecular karyotyping in fetal brain malformations: Identification of novel candidate genes and chromosomal regions.
    Krutzke SK; Engels H; Hofmann A; Schumann MM; Cremer K; Zink AM; Hilger A; Ludwig M; Gembruch U; Reutter H; Merz WM
    Birth Defects Res A Clin Mol Teratol; 2016 Jan; 106(1):16-26. PubMed ID: 26680650
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Copy number variations in ultrasonically abnormal late pregnancy fetuses with normal karyotypes.
    Cai M; Lin N; Su L; Wu X; Xie X; Li Y; Lin Y; Xu L; Huang H
    Sci Rep; 2020 Sep; 10(1):15094. PubMed ID: 32934329
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. Prenatal diagnosis of chromosomal aberrations in fetuses with conotruncal heart defects by genome-wide high-resolution SNP array.
    Lin M; Zheng J; Peng R; Du L; Zheng Q; Lei T; Xie H
    J Matern Fetal Neonatal Med; 2020 Apr; 33(7):1211-1217. PubMed ID: 30149741
    [No Abstract]   [Full Text] [Related]  

  • 17. [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]  

  • 18. [Analysis of genome-wide copy number variations among fetuses with abnormalities detected by prenatal ultrasouography].
    Wu K; Tang S; Chen C; Li H; Zhou L; Lyu J
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr; 34(2):178-182. PubMed ID: 28397213
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Prenatal diagnosis of a fetus with 8q13.3 microdeletion through chromosomal microarray analysis].
    Rao H; Liu Y; Xiao J; Zou Y; Yuan H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Mar; 38(3):268-270. PubMed ID: 33751539
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Assessing the value of second-trimester nasal bone hypoplasia in predicting chromosomal abnormalities: a retrospective chromosomal microarray analysis of 351 fetuses.
    Pan L; Liang H; Meng Z; Wang J; Zhang R; Wu Y
    Arch Gynecol Obstet; 2023 Oct; 308(4):1263-1270. PubMed ID: 36269386
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.