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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 19938088)

  • 1. Goldenhar phenotype in a child with distal 22q11.2 deletion and intracranial atypical teratoid rhabdoid tumor.
    Lafay-Cousin L; Payne E; Strother D; Chernos J; Chan M; Bernier FP
    Am J Med Genet A; 2009 Dec; 149A(12):2855-9. PubMed ID: 19938088
    [TBL] [Abstract][Full Text] [Related]  

  • 2. High-density single nucleotide polymorphism array analysis in patients with germline deletions of 22q11.2 and malignant rhabdoid tumor.
    Jackson EM; Shaikh TH; Gururangan S; Jones MC; Malkin D; Nikkel SM; Zuppan CW; Wainwright LM; Zhang F; Biegel JA
    Hum Genet; 2007 Sep; 122(2):117-27. PubMed ID: 17541642
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Diagnosis of distal 22q11.2 deletion syndrome in a patient with a teratoid/rhabdoid tumour.
    Beddow RA; Smith M; Kidd A; Corbett R; Hunter AG
    Eur J Med Genet; 2011; 54(3):295-8. PubMed ID: 21187175
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney.
    Wieser R; Fritz B; Ullmann R; Müller I; Galhuber M; Storlazzi CT; Ramaswamy A; Christiansen H; Shimizu N; Rehder H
    Hum Mutat; 2005 Aug; 26(2):78-83. PubMed ID: 15957176
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Array analysis and molecular studies of INI1 in an infant with deletion 22q13 (Phelan-McDermid syndrome) and atypical teratoid/rhabdoid tumor.
    Sathyamoorthi S; Morales J; Bermudez J; McBride L; Luquette M; McGoey R; Oates N; Hales S; Biegel JA; Lacassie Y
    Am J Med Genet A; 2009 May; 149A(5):1067-9. PubMed ID: 19334084
    [No Abstract]   [Full Text] [Related]  

  • 6. Distal 22q11.2 microduplication encompassing the BCR gene.
    Descartes M; Franklin J; Diaz de Ståhl T; Piotrowski A; Bruder CE; Dumanski JP; Carroll AJ; Mikhail FM
    Am J Med Genet A; 2008 Dec; 146A(23):3075-81. PubMed ID: 19006218
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Chromosome 22q deletions in atypical teratoid/rhabdoid tumors in adults.
    Raisanen J; Biegel JA; Hatanpaa KJ; Judkins A; White CL; Perry A
    Brain Pathol; 2005 Jan; 15(1):23-8. PubMed ID: 15779233
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Description of a new oncogenic mechanism for atypical teratoid rhabdoid tumors in patients with ring chromosome 22.
    Byers HM; Adam MP; LaCroix A; Leary SE; Cole B; Dobyns WB; Mefford HC
    Am J Med Genet A; 2017 Jan; 173(1):245-249. PubMed ID: 27734605
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Atypical teratoid/rhabdoid tumor of the central nervous system: report on workshop.
    Packer RJ; Biegel JA; Blaney S; Finlay J; Geyer JR; Heideman R; Hilden J; Janss AJ; Kun L; Vezina G; Rorke LB; Smith M
    J Pediatr Hematol Oncol; 2002; 24(5):337-42. PubMed ID: 12142780
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Phenotypic variability of distal 22q11.2 copy number abnormalities.
    Tan TY; Collins A; James PA; McGillivray G; Stark Z; Gordon CT; Leventer RJ; Pope K; Forbes R; Crolla JA; Ganesamoorthy D; Burgess T; Bruno DL; Slater HR; Farlie PG; Amor DJ
    Am J Med Genet A; 2011 Jul; 155A(7):1623-33. PubMed ID: 21671380
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Low copy repeats mediate distal chromosome 22q11.2 deletions: sequence analysis predicts breakpoint mechanisms.
    Shaikh TH; O'Connor RJ; Pierpont ME; McGrath J; Hacker AM; Nimmakayalu M; Geiger E; Emanuel BS; Saitta SC
    Genome Res; 2007 Apr; 17(4):482-91. PubMed ID: 17351135
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Alterations of the hSNF5/INI1 gene in central nervous system atypical teratoid/rhabdoid tumors and renal and extrarenal rhabdoid tumors.
    Biegel JA; Tan L; Zhang F; Wainwright L; Russo P; Rorke LB
    Clin Cancer Res; 2002 Nov; 8(11):3461-7. PubMed ID: 12429635
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Congenital anomalies and rhabdoid tumor associated with 22q11 germline deletion and somatic inactivation of the SMARCB1 tumor suppressor.
    Toth G; Zraly CB; Thomson TL; Jones C; Lapetino S; Muraskas J; Zhang J; Dingwall AK
    Genes Chromosomes Cancer; 2011 Jun; 50(6):379-88. PubMed ID: 21412926
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A child with features of Goldenhar syndrome and a novel 1.12 Mb deletion in 22q11.2 by cytogenetics and oligonucleotide array CGH: is this a candidate region for the syndrome?
    Xu J; Fan YS; Siu VM
    Am J Med Genet A; 2008 Jul; 146A(14):1886-9. PubMed ID: 18553512
    [No Abstract]   [Full Text] [Related]  

  • 15. A complex karyotype in an atypical teratoid/rhabdoid tumor: case report and review of the literature.
    Coccé MC; Lubieniecki F; Kordes U; Alderete D; Gallego MS
    J Neurooncol; 2011 Aug; 104(1):375-80. PubMed ID: 21127945
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ewing Sarcoma and Atypical Teratoid Rhabdoid Tumor: A FISH and Immunohistochemical Comparison.
    Pacheco MC; Dolan M; Bendel A
    Pediatr Dev Pathol; 2017; 20(5):381-386. PubMed ID: 28382842
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Transposable element insertion as a mechanism of SMARCB1 inactivation in atypical teratoid/rhabdoid tumor.
    Thomas C; Oehl-Huber K; Bens S; Soschinski P; Koch A; Nemes K; Oyen F; Kordes U; Kool M; Frühwald MC; Hasselblatt M; Siebert R
    Genes Chromosomes Cancer; 2021 Aug; 60(8):586-590. PubMed ID: 33896072
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Atypical 581-kb 22q11.21 Deletion in a Patient with Oculo-Auriculo-Vertebral Spectrum Phenotype.
    Colovati ME; Bragagnolo S; Guilherme RS; Dantas AG; Soares MF; Kim CA; Perez AB; Melaragno MI
    Cytogenet Genome Res; 2015; 147(2-3):130-4. PubMed ID: 26919065
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients.
    Ensenauer RE; Adeyinka A; Flynn HC; Michels VV; Lindor NM; Dawson DB; Thorland EC; Lorentz CP; Goldstein JL; McDonald MT; Smith WE; Simon-Fayard E; Alexander AA; Kulharya AS; Ketterling RP; Clark RD; Jalal SM
    Am J Hum Genet; 2003 Nov; 73(5):1027-40. PubMed ID: 14526392
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes.
    Ou Z; Berg JS; Yonath H; Enciso VB; Miller DT; Picker J; Lenzi T; Keegan CE; Sutton VR; Belmont J; Chinault AC; Lupski JR; Cheung SW; Roeder E; Patel A
    Genet Med; 2008 Apr; 10(4):267-77. PubMed ID: 18414210
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.