155 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]
