BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

220 related articles for article (PubMed ID: 18285835)

  • 21. Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation.
    Stankiewicz P; Beaudet AL
    Curr Opin Genet Dev; 2007 Jun; 17(3):182-92. PubMed ID: 17467974
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Molecular karyotyping in 17 patients and mutation screening in 41 patients with Kabuki syndrome.
    Kuniba H; Yoshiura K; Kondoh T; Ohashi H; Kurosawa K; Tonoki H; Nagai T; Okamoto N; Kato M; Fukushima Y; Kaname T; Naritomi K; Matsumoto T; Moriuchi H; Kishino T; Kinoshita A; Miyake N; Matsumoto N; Niikawa N
    J Hum Genet; 2009 May; 54(5):304-9. PubMed ID: 19343044
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genomewide screening of DNA copy number changes in chronic myelogenous leukemia with the use of high-resolution array-based comparative genomic hybridization.
    Hosoya N; Sanada M; Nannya Y; Nakazaki K; Wang L; Hangaishi A; Kurokawa M; Chiba S; Ogawa S
    Genes Chromosomes Cancer; 2006 May; 45(5):482-94. PubMed ID: 16425296
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Detecting sex chromosome anomalies and common triploidies in products of conception by array-based comparative genomic hybridization.
    Ballif BC; Kashork CD; Saleki R; Rorem E; Sundin K; Bejjani BA; Shaffer LG
    Prenat Diagn; 2006 Apr; 26(4):333-9. PubMed ID: 16491513
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Array-based comparative genomic hybridization in clinical diagnosis.
    Bejjani BA; Theisen AP; Ballif BC; Shaffer LG
    Expert Rev Mol Diagn; 2005 May; 5(3):421-9. PubMed ID: 15934818
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Detection of a copy number mutation on chromosome 7q36 using the Affymetrix SNP Array 6.0].
    Ma F; Wu FX; Li N; Liu Q; Yang W; Zhang X; Sun M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):336-9. PubMed ID: 19504452
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridization.
    Fan YS; Jayakar P; Zhu H; Barbouth D; Sacharow S; Morales A; Carver V; Benke P; Mundy P; Elsas LJ
    Hum Mutat; 2007 Nov; 28(11):1124-32. PubMed ID: 17621639
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Molecular karyotyping using an SNP array for genomewide genotyping.
    Rauch A; Rüschendorf F; Huang J; Trautmann U; Becker C; Thiel C; Jones KW; Reis A; Nürnberg P
    J Med Genet; 2004 Dec; 41(12):916-22. PubMed ID: 15591277
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization.
    del Gaudio D; Yang Y; Boggs BA; Schmitt ES; Lee JA; Sahoo T; Pham HT; Wiszniewska J; Chinault AC; Beaudet AL; Eng CM
    Hum Mutat; 2008 Sep; 29(9):1100-7. PubMed ID: 18752307
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Across array comparative genomic hybridization: a strategy to reduce reference channel hybridizations.
    Buffart TE; Israeli D; Tijssen M; Vosse SJ; Mrsić A; Meijer GA; Ylstra B
    Genes Chromosomes Cancer; 2008 Nov; 47(11):994-1004. PubMed ID: 18663753
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Cross-platform array comparative genomic hybridization meta-analysis separates hematopoietic and mesenchymal from epithelial tumors.
    Jong K; Marchiori E; van der Vaart A; Chin SF; Carvalho B; Tijssen M; Eijk PP; van den Ijssel P; Grabsch H; Quirke P; Oudejans JJ; Meijer GA; Caldas C; Ylstra B
    Oncogene; 2007 Mar; 26(10):1499-506. PubMed ID: 16936777
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Molecular karyotyping: array CGH quality criteria for constitutional genetic diagnosis.
    Vermeesch JR; Melotte C; Froyen G; Van Vooren S; Dutta B; Maas N; Vermeulen S; Menten B; Speleman F; De Moor B; Van Hummelen P; Marynen P; Fryns JP; Devriendt K
    J Histochem Cytochem; 2005 Mar; 53(3):413-22. PubMed ID: 15750031
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Identification of gene copy number variations in patients with mental retardation using array-CGH: Novel syndromes in a large French series.
    Jaillard S; Drunat S; Bendavid C; Aboura A; Etcheverry A; Journel H; Delahaye A; Pasquier L; Bonneau D; Toutain A; Burglen L; Guichet A; Pipiras E; Gilbert-Dussardier B; Benzacken B; Martin-Coignard D; Henry C; David A; Lucas J; Mosser J; David V; Odent S; Verloes A; Dubourg C
    Eur J Med Genet; 2010; 53(2):66-75. PubMed ID: 19878743
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Genomic microarrays in clinical diagnosis.
    Veltman JA
    Curr Opin Pediatr; 2006 Dec; 18(6):598-603. PubMed ID: 17099357
    [TBL] [Abstract][Full Text] [Related]  

  • 37. MAPH: from gels to microarrays.
    Patsalis PC; Kousoulidou L; Sismani C; Männik K; Kurg A
    Eur J Med Genet; 2005; 48(3):241-9. PubMed ID: 16179220
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Molecular karyotyping of patients with unexplained mental retardation by SNP arrays: a multicenter study.
    McMullan DJ; Bonin M; Hehir-Kwa JY; de Vries BB; Dufke A; Rattenberry E; Steehouwer M; Moruz L; Pfundt R; de Leeuw N; Riess A; Altug-Teber O; Enders H; Singer S; Grasshoff U; Walter M; Walker JM; Lamb CV; Davison EV; Brueton L; Riess O; Veltman JA
    Hum Mutat; 2009 Jul; 30(7):1082-92. PubMed ID: 19388127
    [TBL] [Abstract][Full Text] [Related]  

  • 39. SNP array analysis in constitutional and cancer genome diagnostics--copy number variants, genotyping and quality control.
    de Leeuw N; Hehir-Kwa JY; Simons A; Geurts van Kessel A; Smeets DF; Faas BH; Pfundt R
    Cytogenet Genome Res; 2011; 135(3-4):212-21. PubMed ID: 21934286
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Bacterial artificial chromosome array-based comparative genomic hybridization using paired formalin-fixed, paraffin-embedded and fresh frozen tissue specimens in multiple myeloma.
    Lennon PA; Zhuang Y; Pierson D; Zhang X; Williams C; Perez C; Lin P
    Cancer; 2009 Jan; 115(2):345-54. PubMed ID: 19109814
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.