BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

153 related articles for article (PubMed ID: 19009552)

  • 1. High-resolution array genomic hybridization in prenatal diagnosis.
    Friedman JM
    Prenat Diagn; 2009 Jan; 29(1):20-8. PubMed ID: 19009552
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Fetal chromosome technique by microarray-based comparative genomic hybridization].
    Jonveaux P
    Arch Pediatr; 2010 Jul; 17(7):1119-23. PubMed ID: 20347579
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The impact of array genomic hybridization on mental retardation research: a review of current technologies and their clinical utility.
    Zahir F; Friedman JM
    Clin Genet; 2007 Oct; 72(4):271-87. PubMed ID: 17850622
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Applications of array comparative genomic hybridization in obstetrics.
    Fruhman G; Van den Veyver IB
    Obstet Gynecol Clin North Am; 2010 Mar; 37(1):71-85, Table of Contents. PubMed ID: 20494259
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice.
    Bruno DL; Ganesamoorthy D; Schoumans J; Bankier A; Coman D; Delatycki M; Gardner RJ; Hunter M; James PA; Kannu P; McGillivray G; Pachter N; Peters H; Rieubland C; Savarirayan R; Scheffer IE; Sheffield L; Tan T; White SM; Yeung A; Bowman Z; Ngo C; Choy KW; Cacheux V; Wong L; Amor DJ; Slater HR
    J Med Genet; 2009 Feb; 46(2):123-31. PubMed ID: 19015223
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Computational methods for identification of recurrent copy number alteration patterns by array CGH.
    Shah SP
    Cytogenet Genome Res; 2008; 123(1-4):343-51. PubMed ID: 19287173
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The array CGH and its clinical applications.
    Shinawi M; Cheung SW
    Drug Discov Today; 2008 Sep; 13(17-18):760-70. PubMed ID: 18617013
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Array comparative genomic hybridization in prenatal diagnosis: another experience.
    Vialard F; Molina Gomes D; Leroy B; Quarello E; Escalona A; Le Sciellour C; Serazin V; Roume J; Ville Y; de Mazancourt P; Selva J
    Fetal Diagn Ther; 2009; 25(2):277-84. PubMed ID: 19521095
    [TBL] [Abstract][Full Text] [Related]  

  • 9. High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease.
    Erdogan F; Larsen LA; Zhang L; Tümer Z; Tommerup N; Chen W; Jacobsen JR; Schubert M; Jurkatis J; Tzschach A; Ropers HH; Ullmann R
    J Med Genet; 2008 Nov; 45(11):704-9. PubMed ID: 18713793
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The impact of human copy number variation on a new era of genetic testing.
    Choy KW; Setlur SR; Lee C; Lau TK
    BJOG; 2010 Mar; 117(4):391-8. PubMed ID: 20105165
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Copy number imbalances detected with a BAC-based array comparative genomic hybridization platform in congenital diaphragmatic hernia fetuses.
    Machado IN; Heinrich JK; Barini R; Peralta CF
    Genet Mol Res; 2011 Feb; 10(1):261-7. PubMed ID: 21341218
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray.
    Coppinger J; Alliman S; Lamb AN; Torchia BS; Bejjani BA; Shaffer LG
    Prenat Diagn; 2009 Dec; 29(12):1156-66. PubMed ID: 19795450
    [TBL] [Abstract][Full Text] [Related]  

  • 13. De novo 16p13.11 microdeletion identified by high-resolution array CGH in a fetus with increased nuchal translucency.
    Law LW; Lau TK; Fung TY; Leung TY; Wang CC; Choy KW
    BJOG; 2009 Jan; 116(2):339-43. PubMed ID: 19018765
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Array-based comparative genomic hybridization detection of copy number variations in a fetus with hypoplastic left-heart syndrome].
    Wang Y; Ma DY; Yang YQ; Zhou J; Zhou XY; Ji XQ; Chen J; Cao L; Hu P; Xu ZF
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Aug; 29(4):439-42. PubMed ID: 22875502
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Evolution of prenatal genetics: from point mutation testing to chromosomal microarray analysis.
    Roa BB; Pulliam J; Eng CM; Cheung SW
    Expert Rev Mol Diagn; 2005 Nov; 5(6):883-92. PubMed ID: 16255630
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genomic changes detected by array CGH in human embryos with developmental defects.
    Rajcan-Separovic E; Qiao Y; Tyson C; Harvard C; Fawcett C; Kalousek D; Stephenson M; Philipp T
    Mol Hum Reprod; 2010 Feb; 16(2):125-34. PubMed ID: 19778950
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical utility of array CGH for the detection of chromosomal imbalances associated with mental retardation and multiple congenital anomalies.
    Edelmann L; Hirschhorn K
    Ann N Y Acad Sci; 2009 Jan; 1151():157-66. PubMed ID: 19154522
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis using combined quantitative fluorescent polymerase chain reaction and array comparative genomic hybridization analysis as a first-line test: results from over 1000 consecutive cases.
    Scott F; Murphy K; Carey L; Greville W; Mansfield N; Barahona P; Robertson R; McLennan A
    Ultrasound Obstet Gynecol; 2013 May; 41(5):500-7. PubMed ID: 23401365
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens.
    Shaffer LG; Coppinger J; Alliman S; Torchia BA; Theisen A; Ballif BC; Bejjani BA
    Prenat Diagn; 2008 Sep; 28(9):789-95. PubMed ID: 18646242
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybridization.
    Cho SC; Yim SH; Yoo HK; Kim MY; Jung GY; Shin GW; Kim BN; Hwang JW; Kang JJ; Kim TM; Chung YJ
    Psychiatr Genet; 2009 Aug; 19(4):177-85. PubMed ID: 19407672
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.