BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

82 related articles for article (PubMed ID: 27264809)

  • 1. [Application of chromosome microarray analysis for patients with skeletal anomalies and a normal karyotype].
    Guo Q; Fu F; Li R; Zhang Y; Yang X; Han J; Pan M; Zhen L; Liao C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Jun; 33(3):306-11. PubMed ID: 27264809
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Analysis of 22 patients with congenital cleft lip and palate using high-resolution chromosome microarray].
    Lei T; Zhang Y; Wang H; Li F; Cui Y; Fu F; Li R; Xie G; Zhang Y; Liao C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Aug; 31(4):433-7. PubMed ID: 25119905
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. [Application of chromosome microarray analysis in 489 children with developmental delay/intellectual disability].
    Wang R; Lei T; Fu F; Li R; Jing X; Yang X; Pan M; Li D; Liao C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Aug; 34(4):528-533. PubMed ID: 28777852
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. [Application of chromosomal microarray analysis for fetuses with ventricular septal defects].
    Deng Q; Fu F; Li R; Jing X; Lei T; Yang X; Pan M; Zhen L; Han J; Liao C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Oct; 34(5):699-704. PubMed ID: 28981937
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Application of chromosomal microarray analysis for fetuses with talipes equinovarus].
    Guo QL; Fu F; Li R; Jing XY; Lei TY; Han J; Yang X; Zhen L; Pan M; Liao C
    Zhonghua Fu Chan Ke Za Zhi; 2016 Jul; 51(7):484-90. PubMed ID: 27465866
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Chromosome microarray analysis of patients with 18q deletion syndrome].
    Feng J; Hao J; Chen Y; Li F; Han J; Li R; Zhang Y; Lei T; Chen F; Guo Q; Liao C; Wang H
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):203-7. PubMed ID: 27060316
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Analysis of copy number variations in 66 children with unexplained mental retardation/developmental delay using chromosomal microarrays].
    Li Y; Qiu W; Ye J; Han L; Zhang H; Gu X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Dec; 31(6):703-7. PubMed ID: 25449071
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Application of chromosome microarray analysis for the delineation of pathogenesis for fetal ventriculomegaly].
    Li Z; Fu F; Lei T; Li R; Jing X; Yang X; Han J; Pan M; Zhen L; Liao C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Aug; 34(4):576-582. PubMed ID: 28777863
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Additional cryptic CNVs in mentally retarded patients with apparently balanced karyotypes.
    Gijsbers AC; Bosch CA; Dauwerse JG; Giromus O; Hansson K; Hilhorst-Hofstee Y; Kriek M; van Haeringen A; Bijlsma EK; Bakker E; Breuning MH; Ruivenkamp CA
    Eur J Med Genet; 2010; 53(5):227-33. PubMed ID: 20542150
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Using a combination of MLPA kits to detect chromosomal imbalances in patients with multiple congenital anomalies and mental retardation is a valuable choice for developing countries.
    Jehee FS; Takamori JT; Medeiros PF; Pordeus AC; Latini FR; Bertola DR; Kim CA; Passos-Bueno MR
    Eur J Med Genet; 2011; 54(4):e425-32. PubMed ID: 21457803
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Chromosomal microaberrations in patients with epilepsy, intellectual disability, and congenital anomalies.
    Spreiz A; Haberlandt E; Baumann M; Baumgartner Sigl S; Fauth C; Gautsch K; Karall D; Janetschek C; Rostasy K; Scholl-Bürgi S; Zotter S; Utermann G; Zschocke J; Kotzot D
    Clin Genet; 2014 Oct; 86(4):361-6. PubMed ID: 24116836
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detection of submicroscopic chromosomal aberrations by array-based comparative genomic hybridization in fetuses with congenital heart disease.
    Yan Y; Wu Q; Zhang L; Wang X; Dan S; Deng D; Sun L; Yao L; Ma Y; Wang L
    Ultrasound Obstet Gynecol; 2014 Apr; 43(4):404-12. PubMed ID: 24323407
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Application of chromosome microarray analysis for fetuses with multicystic dysplastic kidney].
    Chen F; Lei T; Fu F; Li R; Zhang Y; Jing X; Yang X; Han J; Zhen L; Pan M; Liao C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Dec; 33(6):752-757. PubMed ID: 27984599
    [TBL] [Abstract][Full Text] [Related]  

  • 16. High resolution chromosomal microarray in undiagnosed neurological disorders.
    Howell KB; Kornberg AJ; Harvey AS; Ryan MM; Mackay MT; Freeman JL; Rodriguez Casero MV; Collins KJ; Hayman M; Mohamed A; Ware TL; Clark D; Bruno DL; Burgess T; Slater H; McGillivray G; Leventer RJ
    J Paediatr Child Health; 2013 Sep; 49(9):716-24. PubMed ID: 23731025
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Application of chromosomal microarray analysis for the diagnosis of children with intellectual disability/developmental delay and a normal karytype].
    Hu T; Zhu H; Zhang Z; Wang J; Liu H; Zhang X; Zhang H; Du Z; Li L; Wang H; Liu S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr; 34(2):169-172. PubMed ID: 28397211
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Application of SNP-array technology in the genetic analysis of pediatric patients with growth retardation].
    Luo S; Fu C; Zhang S; Wang J; Fan X; Luo J; Chen R; Hu X; Qin H; Li C; Ou S; Li Q; Chen S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Jun; 34(3):321-326. PubMed ID: 28604947
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Structural genomic variation in intellectual disability.
    Pfundt R; Veltman JA
    Methods Mol Biol; 2012; 838():77-95. PubMed ID: 22228007
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Karyotype versus microarray testing for genetic abnormalities after stillbirth.
    Reddy UM; Page GP; Saade GR; Silver RM; Thorsten VR; Parker CB; Pinar H; Willinger M; Stoll BJ; Heim-Hall J; Varner MW; Goldenberg RL; Bukowski R; Wapner RJ; Drews-Botsch CD; O'Brien BM; Dudley DJ; Levy B;
    N Engl J Med; 2012 Dec; 367(23):2185-93. PubMed ID: 23215556
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.