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.
2. Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGH. Jarbo C; Buckley PG; Piotrowski A; Mantripragada KK; Benetkiewicz M; Diaz de Ståhl T; Langford CF; Gregory SG; Dralle H; Gimm O; Bäckdahl M; Geli J; Larsson C; Westin G; Akerström G; Dumanski JP Int J Cancer; 2006 Mar; 118(5):1159-64. PubMed ID: 16161042 [TBL] [Abstract][Full Text] [Related]
3. Comparative genomic hybridization analysis of genomic alterations in benign, atypical and anaplastic meningiomas. Arslantas A; Artan S; Oner U; Durmaz R; Müslümanoğlu H; Atasoy MA; Başaran N; Tel E Acta Neurol Belg; 2002 Jun; 102(2):53-62. PubMed ID: 12161900 [TBL] [Abstract][Full Text] [Related]
4. Identification of limited regions of genetic aberrations in patients affected with Wilms' tumor using a tiling-path chromosome 22 array. Benetkiewicz M; Díaz de Ståhl T; Gördör A; Pfeifer S; Wittmann S; Gessler M; Dumanski JP Int J Cancer; 2006 Aug; 119(3):571-8. PubMed ID: 16496407 [TBL] [Abstract][Full Text] [Related]
5. Altered DNA copy number in patients with different seizure disorder type: by array-CGH. Kim HS; Yim SV; Jung KH; Zheng LT; Kim YH; Lee KH; Chung SY; Rha HK Brain Dev; 2007 Nov; 29(10):639-43. PubMed ID: 17573221 [TBL] [Abstract][Full Text] [Related]
6. Array-based comparative genomic hybridization of mapped BAC DNA clones to screen for chromosome 14 copy number abnormalities in meningiomas. Espinosa AB; Mackintosh C; Maíllo A; Gutierrez L; Sousa P; Merino M; Ortiz J; de Alava E; Orfao A; Tabernero MD Eur J Hum Genet; 2008 Dec; 16(12):1450-8. PubMed ID: 18628790 [TBL] [Abstract][Full Text] [Related]
7. Comprehensive DNA copy number profiling of meningioma using a chromosome 1 tiling path microarray identifies novel candidate tumor suppressor loci. Buckley PG; Jarbo C; Menzel U; Mathiesen T; Scott C; Gregory SG; Langford CF; Dumanski JP Cancer Res; 2005 Apr; 65(7):2653-61. PubMed ID: 15805262 [TBL] [Abstract][Full Text] [Related]
9. Copy number variations in Saudi family with intellectual disability and epilepsy. Naseer MI; Chaudhary AG; Rasool M; Kalamegam G; Ashgan FT; Assidi M; Ahmed F; Ansari SA; Zaidi SK; Jan MM; Al-Qahtani MH BMC Genomics; 2016 Oct; 17(Suppl 9):757. PubMed ID: 27766957 [TBL] [Abstract][Full Text] [Related]
10. Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities. Lapierre JM; Cacheux V; Collot N; Da Silva F; Hervy N; Rivet D; Romana S; Wiss J; Benzaken B; Aurias A; Tachdjian G Ann Genet; 1998; 41(3):133-40. PubMed ID: 9833066 [TBL] [Abstract][Full Text] [Related]
11. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays. Pinkel D; Segraves R; Sudar D; Clark S; Poole I; Kowbel D; Collins C; Kuo WL; Chen C; Zhai Y; Dairkee SH; Ljung BM; Gray JW; Albertson DG Nat Genet; 1998 Oct; 20(2):207-11. PubMed ID: 9771718 [TBL] [Abstract][Full Text] [Related]
13. Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects. Hussein IR; Bader RS; Chaudhary AG; Bassiouni R; Alquaiti M; Ashgan F; Schulten HJ; Al Qahtani MH Pediatr Cardiol; 2018 Jun; 39(5):924-940. PubMed ID: 29541814 [TBL] [Abstract][Full Text] [Related]
14. Array comparative genomic hybridization analysis of chromosomal imbalances and their target genes in gastrointestinal stromal tumors. Assämäki R; Sarlomo-Rikala M; Lopez-Guerrero JA; Lasota J; Andersson LC; Llombart-Bosch A; Miettinen M; Knuutila S Genes Chromosomes Cancer; 2007 Jun; 46(6):564-76. PubMed ID: 17330260 [TBL] [Abstract][Full Text] [Related]
15. Copy number alterations in small intestinal neuroendocrine tumors determined by array comparative genomic hybridization. Hashemi J; Fotouhi O; Sulaiman L; Kjellman M; Höög A; Zedenius J; Larsson C BMC Cancer; 2013 Oct; 13():505. PubMed ID: 24165089 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. [Genomic profiling: from molecular cytogenetics to DNA arrays]. Theillet C; Orsetti B; Redon R; Manoir SD Bull Cancer; 2001 Mar; 88(3):261-8. PubMed ID: 11313203 [TBL] [Abstract][Full Text] [Related]
18. Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors. Kallioniemi OP; Kallioniemi A; Piper J; Isola J; Waldman FM; Gray JW; Pinkel D Genes Chromosomes Cancer; 1994 Aug; 10(4):231-43. PubMed ID: 7522536 [TBL] [Abstract][Full Text] [Related]
19. Comparative genomic hybridization and its application to Wilms' tumorigenesis. Getman ME; Houseal TW; Miller GA; Grundy PE; Cowell JK; Landes GM Cytogenet Cell Genet; 1998; 82(3-4):284-90. PubMed ID: 9858837 [TBL] [Abstract][Full Text] [Related]