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 *

208 related articles for article (PubMed ID: 28397212)

  • 1. [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]  

  • 2. [Prenatal diagnosis of women with an adverse reproductive history using both traditional karyotyping and SNP-array].
    Yu HS; Guo H; Shen SS; Li XC; Zhang LP; Fan XF
    Zhonghua Fu Chan Ke Za Zhi; 2018 Mar; 53(3):155-159. PubMed ID: 29609228
    [No Abstract]   [Full Text] [Related]  

  • 3. [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]  

  • 4. [Clinical significance of secondary results from non-invasive prenatal testing].
    Ke W; Zhao W; Jie S; Chen Q; Li Q
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Jun; 34(3):327-331. PubMed ID: 28604948
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Application of chromosome microarray analysis for fetuses with increased nuchal translucency and a normal karyotype].
    Yang X; Fu F; Li R; Zhang Y; Wan J; Yang X; Han J; Pan M; Zhen L; Liao C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Jun; 32(3):370-4. PubMed ID: 26037353
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical application of SNP array analysis in fetuses with ventricular septal defects and normal karyotypes.
    Fu F; Deng Q; Lei TY; Li R; Jing XY; Yang X; Liao C
    Arch Gynecol Obstet; 2017 Nov; 296(5):929-940. PubMed ID: 28905115
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. [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]  

  • 9. [Combined G-banded karyotyping and multiplex ligation-dependent probe amplification for the detection of chromosomal abnormalities in fetuses with congenital heart defects].
    Liu Y; Xie J; Geng Q; Xu Z; Wu W; Luo F; Li S; Wang Q; Chen W; Tan H; Zhang H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):1-5. PubMed ID: 28186583
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Copy number variation sequencing-based prenatal diagnosis using cell-free fetal DNA in amniotic fluid.
    Qi Q; Lu S; Zhou X; Yao F; Hao N; Yin G; Li W; Bai J; Li N; Cram DS
    Prenat Diagn; 2016 Jun; 36(6):576-83. PubMed ID: 27084671
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cell-free DNA test for pathogenic copy number variations: A retrospective study.
    Duan HL; Li J; Wang WJ; Cram DS; Liu W; Cao PX; Zhu XY; Hu YL
    Taiwan J Obstet Gynecol; 2021 Nov; 60(6):1066-1071. PubMed ID: 34794739
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Analysis of genomic copy number variations in fetuses with conotruncal defects using single nucleotide polymorphism array].
    Wang J; Zhao Y; Jin H; Tao J; Cao L; Cai Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Jun; 35(3):347-350. PubMed ID: 29896729
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Prenatal diagnosis of a rare case of 7q11.23 duplication syndrome].
    Ma G; Jiang Y; Yu Z; Dai W; Liu N; Li H; Mijiti G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr; 34(2):244-246. PubMed ID: 28397229
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dilemmas in genetic counseling for low-penetrance neuro-susceptibility loci detected on prenatal chromosomal microarray analysis.
    Brabbing-Goldstein D; Reches A; Svirsky R; Bar-Shira A; Yaron Y
    Am J Obstet Gynecol; 2018 Feb; 218(2):247.e1-247.e12. PubMed ID: 29146387
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Application of chromosomal microarray analysis in prenatal diagnosis for fetal abnormalities detected by ultrasonography].
    Hu T; Wang J; Zhang Z; Zhu H; Liu H; Zhang X; Zhang H; Du Z; Li L; Wang H; Liu S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Jun; 34(3):317-320. PubMed ID: 28604946
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Fetal congenital heart disease: Associated anomalies, identification of genetic anomalies by single-nucleotide polymorphism array analysis, and postnatal outcome.
    Cai M; Huang H; Su L; Lin N; Wu X; Xie X; An G; Li Y; Lin Y; Xu L
    Medicine (Baltimore); 2018 Dec; 97(50):e13617. PubMed ID: 30558042
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Applied research of combined G-banding and array-CGH in the prenatal diagnosis of ultrasonographic abnormalities in fetuses].
    Fu W; Lu J; Xu L; Zheng L; Zhang Y; Zhong Y; Wang Y; Jin Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):737-42. PubMed ID: 25449078
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotype.
    Leung TY; Vogel I; Lau TK; Chong W; Hyett JA; Petersen OB; Choy KW
    Ultrasound Obstet Gynecol; 2011 Sep; 38(3):314-9. PubMed ID: 21400624
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.