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Integrative genomics identifies distinct molecular classes of neuroblastoma and shows that multiple genes are targeted by regional alterations in DNA copy number.
Cancer Res. 2006 Jun 15;66(12):6050-62. doi: 10.1158/0008-5472.CAN-05-4618.
Cancer Res. 2006.
PMID: 16778177
Detection of single-copy chromosome 17q gain in human neuroblastomas using real-time quantitative polymerase chain reaction.
Morowitz M, Shusterman S, Mosse Y, Hii G, Winter CL, Khazi D, Wang Q, King R, Maris JM.
Morowitz M, et al. Among authors: khazi d.
Mod Pathol. 2003 Dec;16(12):1248-56. doi: 10.1097/01.MP.0000097364.64566.81.
Mod Pathol. 2003.
PMID: 14681326
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High-resolution detection and mapping of genomic DNA alterations in neuroblastoma.
Mosse YP, Greshock J, Margolin A, Naylor T, Cole K, Khazi D, Hii G, Winter C, Shahzad S, Asziz MU, Biegel JA, Weber BL, Maris JM.
Mosse YP, et al. Among authors: khazi d.
Genes Chromosomes Cancer. 2005 Aug;43(4):390-403. doi: 10.1002/gcc.20198.
Genes Chromosomes Cancer. 2005.
PMID: 15892104
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Chromosome 1p and 11q deletions and outcome in neuroblastoma.
Attiyeh EF, London WB, Mossé YP, Wang Q, Winter C, Khazi D, McGrady PW, Seeger RC, Look AT, Shimada H, Brodeur GM, Cohn SL, Matthay KK, Maris JM; Children's Oncology Group.
Attiyeh EF, et al. Among authors: khazi d.
N Engl J Med. 2005 Nov 24;353(21):2243-53. doi: 10.1056/NEJMoa052399.
N Engl J Med. 2005.
PMID: 16306521
Free article.
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Identification and high-resolution mapping of a constitutional 11q deletion in an infant with multifocal neuroblastoma.
Mosse Y, Greshock J, King A, Khazi D, Weber BL, Maris JM.
Mosse Y, et al. Among authors: khazi d.
Lancet Oncol. 2003 Dec;4(12):769-71. doi: 10.1016/s1470-2045(03)01283-x.
Lancet Oncol. 2003.
PMID: 14662434
No abstract available.
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Germline PHOX2B mutation in hereditary neuroblastoma.
Mosse YP, Laudenslager M, Khazi D, Carlisle AJ, Winter CL, Rappaport E, Maris JM.
Mosse YP, et al. Among authors: khazi d.
Am J Hum Genet. 2004 Oct;75(4):727-30. doi: 10.1086/424530.
Am J Hum Genet. 2004.
PMID: 15338462
Free PMC article.
No abstract available.
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