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Items: 1 to 20 of 93

1.

Wilms tumor incidence in children with 2q terminal deletions: a cohort study.

Jones EA, Stewart A, Stiller C, Douglas F, Bown N.

Am J Med Genet A. 2011 Sep;155A(9):2221-3. doi: 10.1002/ajmg.a.34117. Epub 2011 Aug 3.

PMID:
21815249
2.

A cytogenetic study of Wilms' tumor.

Slater RM, de Kraker J, Voƻte PA, Delemarre JF.

Cancer Genet Cytogenet. 1985 Jan 1;14(1-2):95-109.

PMID:
2981155
3.
4.

Prediction by FISH analysis of the occurrence of Wilms tumor in aniridia patients.

Muto R, Yamamori S, Ohashi H, Osawa M.

Am J Med Genet. 2002 Apr 1;108(4):285-9.

PMID:
11920832
5.

Chromosome number 11 and Wilms' tumor.

Slater RM, de Kraker J.

Cancer Genet Cytogenet. 1982 Mar;5(3):237-45.

PMID:
6279277
6.

Chromosome 2q terminal deletion: report of 6 new patients and review of phenotype-breakpoint correlations in 66 individuals.

Casas KA, Mononen TK, Mikail CN, Hassed SJ, Li S, Mulvihill JJ, Lin HJ, Falk RE.

Am J Med Genet A. 2004 Nov 1;130A(4):331-9.

PMID:
15386475
7.

Wilms tumor in a patient with 22q11.2 microdeletion.

Finch PT, Pivnick EK, Furman W, Odom CC.

Am J Med Genet A. 2011 May;155A(5):1162-4. doi: 10.1002/ajmg.a.33957. Epub 2011 Mar 31.

PMID:
21456030
8.

Chromosome analyses of 16 cases of Wilms tumor: different pattern in unfavorable histology.

Peres EM, Savasan S, Cushing B, Abella S, Mohamed AN.

Cancer Genet Cytogenet. 2004 Jan 1;148(1):66-70.

PMID:
14697643
9.

Molecular analysis of aniridia patients for deletions involving the Wilms' tumor gene.

Drechsler M, Meijers-Heijboer EJ, Schneider S, Schurich B, Grond-Ginsbach C, Tariverdian G, Kantner G, Blankenagel A, Kaps D, Schroeder-Kurth T, et al.

Hum Genet. 1994 Oct;94(4):331-8.

PMID:
7927324
10.

Cytogenetic and histologic findings in Wilms' tumor.

Gow KW, Murphy JJ.

J Pediatr Surg. 2002 Jun;37(6):823-7.

PMID:
12037743
11.

Further chromosome studies on Wilms' tumor cells of patients without aniridia.

Kaneko Y, Kondo K, Rowley JD, Moohr JW, Maurer HS.

Cancer Genet Cytogenet. 1983 Oct;10(2):191-7.

PMID:
6311403
12.
13.

Terminal 2q deletion and partial trisomy chromosome 15q: a clinical and cytogenetic study.

El-Bassyouni HT, El-Gerzawy AM, Mohamed AM, Kamel AK, Hussein HA, Thomas MM, El-Ruby M.

Genet Couns. 2014;25(2):151-8. Review.

PMID:
25059013
14.

Correlation of chromosome abnormalities with presence or absence of WT1 deletions/mutations in Wilms tumor.

Nakadate H, Tsuchiya T, Maseki N, Hatae Y, Tsunematsu Y, Horikoshi Y, Ishida Y, Kikuta A, Eguchi H, Endo M, Miyake M, Sakurai M, Kaneko Y.

Genes Chromosomes Cancer. 1999 May;25(1):26-32.

PMID:
10221336
15.

Deletion of WT1 and WIT1 genes and loss of heterozygosity on chromosome 11p in Wilms tumors in Japan.

Kaneko Y, Takeda O, Homma C, Maseki N, Miyoshi H, Tsunematsu Y, Williams BG, Saunders GF, Sakurai M.

Jpn J Cancer Res. 1993 Jun;84(6):616-24.

PMID:
8393432
16.

Cytogenetic changes in Wilms' tumors.

Solis V, Pritchard J, Cowell JK.

Cancer Genet Cytogenet. 1988 Sep;34(2):223-34.

PMID:
2842036
17.

Unbalanced translocation of chromosome 3p in Wilms' tumor.

Walton JM, Lee CL, Mikhail E, Welch JP, Gillis DA.

J Pediatr Surg. 1992 Oct;27(10):1311-4.

PMID:
1328583
18.

Screening for Wilms tumor and hepatoblastoma in children with Beckwith-Wiedemann syndromes: a cost-effective model.

McNeil DE, Brown M, Ching A, DeBaun MR.

Med Pediatr Oncol. 2001 Oct;37(4):349-56.

PMID:
11568898
19.

Segmental haplosufficiency: transmitted deletions of 2p12 include a pancreatic regeneration gene cluster and have no apparent phenotypic consequences.

Barber JC, Thomas NS, Collinson MN, Dennis NR, Liehr T, Weise A, Belitz B, Pfeiffer L, Kirchhoff M, Krag-Olsen B, Lundsteen C.

Eur J Hum Genet. 2005 Mar;13(3):283-91.

20.

Homozygous deletion of a DNA marker from chromosome 11p13 in sporadic Wilms tumor.

Lewis WH, Yeger H, Bonetta L, Chan HS, Kang J, Junien C, Cowell J, Jones C, Dafoe LA.

Genomics. 1988 Jul;3(1):25-31.

PMID:
2851538
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