BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

285 related articles for article (PubMed ID: 16909388)

  • 1. Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation.
    Friedman JM; Baross A; Delaney AD; Ally A; Arbour L; Armstrong L; Asano J; Bailey DK; Barber S; Birch P; Brown-John M; Cao M; Chan S; Charest DL; Farnoud N; Fernandes N; Flibotte S; Go A; Gibson WT; Holt RA; Jones SJ; Kennedy GC; Krzywinski M; Langlois S; Li HI; McGillivray BC; Nayar T; Pugh TJ; Rajcan-Separovic E; Schein JE; Schnerch A; Siddiqui A; Van Allen MI; Wilson G; Yong SL; Zahir F; Eydoux P; Marra MA
    Am J Hum Genet; 2006 Sep; 79(3):500-13. PubMed ID: 16909388
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Whole-genome array-CGH identifies novel contiguous gene deletions and duplications associated with developmental delay, mental retardation, and dysmorphic features.
    Aradhya S; Manning MA; Splendore A; Cherry AM
    Am J Med Genet A; 2007 Jul; 143A(13):1431-41. PubMed ID: 17568414
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular karyotyping in patients with mental retardation using 100K single-nucleotide polymorphism arrays.
    Hoyer J; Dreweke A; Becker C; Göhring I; Thiel CT; Peippo MM; Rauch R; Hofbeck M; Trautmann U; Zweier C; Zenker M; Hüffmeier U; Kraus C; Ekici AB; Rüschendorf F; Nürnberg P; Reis A; Rauch A
    J Med Genet; 2007 Oct; 44(10):629-36. PubMed ID: 17601928
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization.
    Friedman J; Adam S; Arbour L; Armstrong L; Baross A; Birch P; Boerkoel C; Chan S; Chai D; Delaney AD; Flibotte S; Gibson WT; Langlois S; Lemyre E; Li HI; MacLeod P; Mathers J; Michaud JL; McGillivray BC; Patel MS; Qian H; Rouleau GA; Van Allen MI; Yong SL; Zahir FR; Eydoux P; Marra MA
    BMC Genomics; 2009 Nov; 10():526. PubMed ID: 19917086
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features.
    Shaw-Smith C; Redon R; Rickman L; Rio M; Willatt L; Fiegler H; Firth H; Sanlaville D; Winter R; Colleaux L; Bobrow M; Carter NP
    J Med Genet; 2004 Apr; 41(4):241-8. PubMed ID: 15060094
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Genomic abnormalities in children with mental retardation and autism: the use of comparative genomic hybridization in situ (HRCGH) and molecular karyotyping with DNA-microchips (array CGH)].
    Vorsanova SG; Iurov IIu; Kurinnaia OS; Voinova VIu; Iurov IuB
    Zh Nevrol Psikhiatr Im S S Korsakova; 2013; 113(8):46-9. PubMed ID: 24077551
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An oligonucleotide based array-CGH system for detection of genome wide copy number changes including subtelomeric regions for genetic evaluation of mental retardation.
    Toruner GA; Streck DL; Schwalb MN; Dermody JJ
    Am J Med Genet A; 2007 Apr; 143A(8):824-9. PubMed ID: 17366576
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation.
    Tucker T; Montpetit A; Chai D; Chan S; Chénier S; Coe BP; Delaney A; Eydoux P; Lam WL; Langlois S; Lemyre E; Marra M; Qian H; Rouleau GA; Vincent D; Michaud JL; Friedman JM
    BMC Med Genomics; 2011 Mar; 4():25. PubMed ID: 21439053
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A new diagnostic workflow for patients with mental retardation and/or multiple congenital abnormalities: test arrays first.
    Gijsbers AC; Lew JY; Bosch CA; Schuurs-Hoeijmakers JH; van Haeringen A; den Hollander NS; Kant SG; Bijlsma EK; Breuning MH; Bakker E; Ruivenkamp CA
    Eur J Hum Genet; 2009 Nov; 17(11):1394-402. PubMed ID: 19436329
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Whole-genome array-CGH for detection of submicroscopic chromosomal imbalances in children with mental retardation.
    Thuresson AC; Bondeson ML; Edeby C; Ellis P; Langford C; Dumanski JP; Annerén G
    Cytogenet Genome Res; 2007; 118(1):1-7. PubMed ID: 17901693
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Copy-number variations measured by single-nucleotide-polymorphism oligonucleotide arrays in patients with mental retardation.
    Wagenstaller J; Spranger S; Lorenz-Depiereux B; Kazmierczak B; Nathrath M; Wahl D; Heye B; Glaser D; Liebscher V; Meitinger T; Strom TM
    Am J Hum Genet; 2007 Oct; 81(4):768-79. PubMed ID: 17847001
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases.
    Shao L; Shaw CA; Lu XY; Sahoo T; Bacino CA; Lalani SR; Stankiewicz P; Yatsenko SA; Li Y; Neill S; Pursley AN; Chinault AC; Patel A; Beaudet AL; Lupski JR; Cheung SW
    Am J Med Genet A; 2008 Sep; 146A(17):2242-51. PubMed ID: 18663743
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).
    Schoumans J; Ruivenkamp C; Holmberg E; Kyllerman M; Anderlid BM; Nordenskjöld M
    J Med Genet; 2005 Sep; 42(9):699-705. PubMed ID: 16141005
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Analysis of chromosomal aberrations in patients with mental retardation using the array-CGH technique: a single Czech centre experience.
    Zrnová E; Vranová V; Slámová I; Gaillyová R; Kuglík P
    Folia Biol (Praha); 2011; 57(5):206-15. PubMed ID: 22123463
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports.
    Menten B; Maas N; Thienpont B; Buysse K; Vandesompele J; Melotte C; de Ravel T; Van Vooren S; Balikova I; Backx L; Janssens S; De Paepe A; De Moor B; Moreau Y; Marynen P; Fryns JP; Mortier G; Devriendt K; Speleman F; Vermeesch JR
    J Med Genet; 2006 Aug; 43(8):625-33. PubMed ID: 16490798
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Single exon-resolution targeted chromosomal microarray analysis of known and candidate intellectual disability genes.
    Tucker T; Zahir FR; Griffith M; Delaney A; Chai D; Tsang E; Lemyre E; Dobrzeniecka S; Marra M; Eydoux P; Langlois S; Hamdan FF; Michaud JL; Friedman JM
    Eur J Hum Genet; 2014 Jun; 22(6):792-800. PubMed ID: 24253858
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Submicroscopic subtelomeric aberrations in Chinese patients with unexplained developmental delay/mental retardation.
    Wu Y; Ji T; Wang J; Xiao J; Wang H; Li J; Gao Z; Yang Y; Cai B; Wang L; Zhou Z; Tian L; Wang X; Zhong N; Qin J; Wu X; Jiang Y
    BMC Med Genet; 2010 May; 11():72. PubMed ID: 20459802
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Array analysis and karyotyping: workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands.
    Hochstenbach R; van Binsbergen E; Engelen J; Nieuwint A; Polstra A; Poddighe P; Ruivenkamp C; Sikkema-Raddatz B; Smeets D; Poot M
    Eur J Med Genet; 2009; 52(4):161-9. PubMed ID: 19362174
    [TBL] [Abstract][Full Text] [Related]  

  • 19. X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation.
    Madrigal I; Rodríguez-Revenga L; Armengol L; González E; Rodriguez B; Badenas C; Sánchez A; Martínez F; Guitart M; Fernández I; Arranz JA; Tejada M; Pérez-Jurado LA; Estivill X; Milà M
    BMC Genomics; 2007 Nov; 8():443. PubMed ID: 18047645
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Array-based comparative genome hybridization in clinical genetics.
    Bar-Shira A; Rosner G; Rosner S; Goldstein M; Orr-Urtreger A
    Pediatr Res; 2006 Sep; 60(3):353-8. PubMed ID: 16857771
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.