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Items: 1 to 20 of 108

1.

One in 10 million: a case of cleidocranial dysplasia and acute lymphoblastic leukaemia--more than just a coincidence?

Gardham A, Forsythe E, Goulden N.

Clin Dysmorphol. 2012 Jul;21(3):170-1. doi: 10.1097/MCD.0b013e32835431fd. No abstract available.

PMID:
22569278
2.

Prevalence of ETV6-RUNX1 fusion gene in children with acute lymphoblastic leukemia in China.

Gao YJ, Zhu XH, Yang Y, Wu Y, Lu FJ, Zhai XW, Wang HS.

Cancer Genet Cytogenet. 2007 Oct 1;178(1):57-60.

PMID:
17889709
3.

Characterizing chromosomal break points of t(12;21)[ETV6-RUNX1]-positive leukaemia using multiple tiling PCR on whole-genome-amplified DNA.

Lausten-Thomsen U, Madsen HO, Schmiegelow K.

Leukemia. 2010 Jan;24(1):203-5. doi: 10.1038/leu.2009.170. No abstract available.

PMID:
19710699
4.

TEL/AML1-positive patients lacking TEL exon 5 resemble canonical TEL/AML1 cases.

Zaliova M, Meyer C, Cario G, Vaskova M, Marschalek R, Stary J, Zuna J, Trka J.

Pediatr Blood Cancer. 2011 Feb;56(2):217-25. doi: 10.1002/pbc.22686.

PMID:
21157892
5.

Clone-specific secondary aberrations are not detected in neonatal blood spots of children with ETV6-RUNX1-positive leukemia.

Morak M, Meyer C, Marschalek R, Mann G, Haas OA, Panzer-Grümayer R.

Haematologica. 2013 Sep;98(9):e108-10. doi: 10.3324/haematol.2013.090860. No abstract available.

6.

[A case report of childhood acute lymphoblastic leukemia with intrachromosomal amplification of AML1 gene in chromosome 21 and TEL deletion].

Yang W, Xiong F, Huang H, Wu Y, Lin Y, Fan X, Liu Z, Zhang X, Xu H, Zeng H, Zeng S.

Zhonghua Xue Ye Xue Za Zhi. 2015 Jul;36(7):569. doi: 10.3760/cma.j.issn.0253-2727.2015.07.008. Chinese. No abstract available.

PMID:
26304079
7.

The presence of TEL/AML1 rearrangement and cryptic deletion of the TEL gene in adult acute lymphoblastic leukemia (ALL).

Lee DS, Kim YR, Cho HK, Lee CK, Lee JH, Cho HI.

Cancer Genet Cytogenet. 2005 Oct 15;162(2):176-8.

PMID:
16213368
8.

Prospective gene expression analysis accurately subtypes acute leukaemia in children and establishes a commonality between hyperdiploidy and t(12;21) in acute lymphoblastic leukaemia.

van Delft FW, Bellotti T, Luo Z, Jones LK, Patel N, Yiannikouris O, Hill AS, Hubank M, Kempski H, Fletcher D, Chaplin T, Foot N, Young BD, Hann IM, Gammerman A, Saha V.

Br J Haematol. 2005 Jul;130(1):26-35.

PMID:
15982341
9.

Febrile infections in young children do not frequently induce translocation ETV6-RUNX1.

Olsen M, Nielsen NK, Birkballe S, Hjalgrim H, Madsen HO, Schmiegelow K.

Blood Cells Mol Dis. 2011 Feb 15;46(2):175-6. doi: 10.1016/j.bcmd.2010.11.003. No abstract available.

PMID:
21145270
10.

Cleidocranial dysplasia in a Polish population: high frequency of the R193X mutation.

Kisiel BM, Kostrzewa G, Wlasienko P, Kruczek A, Gajdulewicz M, Maciejak D, Wisniewska M, Ploski R, Korniszewski L.

Clin Genet. 2006 Aug;70(2):167-9. No abstract available.

PMID:
16879201
11.

Native ETV6 deletions accompanied by ETV6-RUNX1 rearrangements are associated with a favourable prognosis in childhood acute lymphoblastic leukaemia: a candidate for prognostic marker.

Ko DH, Jeon Y, Kang HJ, Park KD, Shin HY, Kim HK, Cho HI, Ahn HS, Lee DS.

Br J Haematol. 2011 Nov;155(4):530-3. doi: 10.1111/j.1365-2141.2011.08729.x. No abstract available.

PMID:
21569007
12.

[Gene mutation detection in a cleidocranial dysplasia family].

Wang Y, Wu H, Zhang XX, Zhao HS, Feng HL.

Zhonghua Kou Qiang Yi Xue Za Zhi. 2005 Nov;40(6):459-62. Chinese.

PMID:
16329826
13.

Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.

Ellinghaus E, Stanulla M, Richter G, Ellinghaus D, te Kronnie G, Cario G, Cazzaniga G, Horstmann M, Panzer Grümayer R, Cavé H, Trka J, Cinek O, Teigler-Schlegel A, ElSharawy A, Häsler R, Nebel A, Meissner B, Bartram T, Lescai F, Franceschi C, Giordan M, Nürnberg P, Heinzow B, Zimmermann M, Schreiber S, Schrappe M, Franke A.

Leukemia. 2012 May;26(5):902-9. doi: 10.1038/leu.2011.302.

14.

[Comparative study on clinical features between TEL-AML1 positive and negative childhood acute lymphoblastic leukemia].

Guo X, Li Q, Zhu YP, Zhou CY, Gao J, Li XH, Pan LL, Li FY, Tian X, Liu HT.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Oct;24(5):560-3. Chinese.

PMID:
17922427
15.

BCR-ABL, ETV6-RUNX1 and E2A-PBX1: prevalence of the most common acute lymphoblastic leukemia fusion genes in Mexican patients.

Jiménez-Morales S, Miranda-Peralta E, Saldaña-Alvarez Y, Perez-Vera P, Paredes-Aguilera R, Rivera-Luna R, Velázquez-Cruz R, Ramírez-Bello J, Carnevale A, Orozco L.

Leuk Res. 2008 Oct;32(10):1518-22. doi: 10.1016/j.leukres.2008.03.021.

PMID:
18455790
16.

ETV6/RUNX1 fusion lacking prognostic effect in pediatric patients with acute lymphoblastic leukemia.

Zen PR, Capra ME, Silla LM, Loss JF, Fernandes MS, Jacques SM, Paskulin GA.

Cancer Genet Cytogenet. 2009 Jan 15;188(2):112-7. doi: 10.1016/j.cancergencyto.2008.09.005.

PMID:
19100516
17.

Additional aberrations of the ETV6 and RUNX1 genes have no prognostic impact in 229 t(12;21)(p13;q22)-positive B-cell precursor acute lymphoblastic leukaemias treated according to the NOPHO-ALL-2000 protocol.

Barbany G, Andersen MK, Autio K, Borgström G, Franco LC, Golovleva I, Heim S, Heinonen K, Hovland R, Johansson B, Johannsson JH, Kjeldsen E, Nordgren A, Palmqvist L, Forestier E; Nordic Society of Paediatric Haematology and Oncology.; Swedish Cytogenetic Leukaemia Study Group.; NOPHO Leukaemia Cytogenetic Study Group..

Leuk Res. 2012 Jul;36(7):936-8. doi: 10.1016/j.leukres.2012.03.024. No abstract available.

PMID:
22521551
18.

[Cytogenetic and FISH findings are complementary in childhood ALL].

Haltrich I, Csóka M, Kovács G, Fekete G.

Magy Onkol. 2008 Sep;52(3):283-91. doi: 10.1556/MOnkol.52.2008.3.6. Hungarian.

PMID:
18845499
19.

Adult acute leukemia.

Cornell RF, Palmer J.

Dis Mon. 2012 Apr;58(4):219-38. doi: 10.1016/j.disamonth.2012.01.011. Review. No abstract available.

PMID:
22449370
20.

The presence of germ line mosaicism in cleidocranial dysplasia.

Pal T, Napierala D, Becker TA, Loscalzo M, Baldridge D, Lee B, Sutphen R.

Clin Genet. 2007 Jun;71(6):589-91.

PMID:
17539909
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