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Items: 1 to 20 of 58

1.

The segregation of different submicroscopic imbalances underlying the clinical variability associated with a familial karyotypically balanced translocation.

Fonseca AC, Bonaldi A, Fonseca SA, Otto PA, Kok F, Bak M, Tommerup N, Vianna-Morgante AM.

Mol Cytogenet. 2015 Dec 30;8:106. doi: 10.1186/s13039-015-0205-9. eCollection 2015.

2.

Balanced complex chromosome rearrangement in male infertility: case report and literature review.

Nguyen MH, Morel F, Pennamen P, Parent P, Douet-Guilbert N, Le Bris MJ, Basinko A, Roche S, De Braekeleer M, Perrin A.

Andrologia. 2015 Mar;47(2):178-85. doi: 10.1111/and.12245. Epub 2014 Feb 24. Review.

PMID:
24612408
3.

A coalescence of two syndromes in a girl with terminal deletion and inverted duplication of chromosome 5.

Krgovic D, Blatnik A, Burmas A, Zagorac A, Kokalj Vokac N.

BMC Med Genet. 2014 Feb 11;15:21. doi: 10.1186/1471-2350-15-21.

4.

NUP98/JARID1A is a novel recurrent abnormality in pediatric acute megakaryoblastic leukemia with a distinct HOX gene expression pattern.

de Rooij JD, Hollink IH, Arentsen-Peters ST, van Galen JF, Berna Beverloo H, Baruchel A, Trka J, Reinhardt D, Sonneveld E, Zimmermann M, Alonzo TA, Pieters R, Meshinchi S, van den Heuvel-Eibrink MM, Zwaan CM.

Leukemia. 2013 Dec;27(12):2280-8. doi: 10.1038/leu.2013.87. Epub 2013 Mar 27.

PMID:
23531517
5.

Isochromosome 5p and related anomalies: a novel recurrent chromosome abnormality in myeloid disorders.

Herry A, Douet-Guilbert N, Morel F, Le Bris MJ, Guéganic N, Berthou C, De Braekeleer M.

Cancer Genet Cytogenet. 2010 Jul 15;200(2):134-9. doi: 10.1016/j.cancergencyto.2010.04.006.

PMID:
20620596
6.

Craniosynostosis in a patient with 2q37.3 deletion 5q34 duplication: association of extra copy of MSX2 with craniosynostosis.

Kariminejad A, Kariminejad R, Tzschach A, Ullmann R, Ahmed A, Asghari-Roodsari A, Salehpour S, Afroozan F, Ropers HH, Kariminejad MH.

Am J Med Genet A. 2009 Jul;149A(7):1544-9. doi: 10.1002/ajmg.a.32949.

PMID:
19533795
8.

Replication-timing-correlated spatial chromatin arrangements in cancer and in primate interphase nuclei.

Grasser F, Neusser M, Fiegler H, Thormeyer T, Cremer M, Carter NP, Cremer T, Müller S.

J Cell Sci. 2008 Jun 1;121(11):1876-86. doi: 10.1242/jcs.026989. Epub 2008 May 13.

9.

Inverted duplication with terminal deletion of 5p and no cat-like cry.

Wang JC, Coe BP, Lomax B, MacLeod PM, Parslow MI, Schein JE, Lam WL, Eydoux P.

Am J Med Genet A. 2008 May 1;146A(9):1173-9. doi: 10.1002/ajmg.a.32246.

PMID:
18266247
10.

Late-appearing pseudocentric fission event during chronic myeloid leukemia progression.

Storlazzi CT, Albano F, Dencić-Fekete M, Djordjević V, Rocchi M.

Cancer Genet Cytogenet. 2007 Apr 1;174(1):61-7.

PMID:
17350469
11.

Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32-->q33 and 12q14-->q15.

Nilsson M, Mertens F, Höglund M, Mandahl N, Panagopoulos I.

Cytogenet Genome Res. 2006;112(1-2):60-6.

PMID:
16276091
12.

Role of nucleophosmin in embryonic development and tumorigenesis.

Grisendi S, Bernardi R, Rossi M, Cheng K, Khandker L, Manova K, Pandolfi PP.

Nature. 2005 Sep 1;437(7055):147-53. Epub 2005 Jul 6.

13.
14.

A new complex rearrangement involving the ETV6, LOC115548, and MN1 genes in a case of acute myeloid leukemia.

Belloni E, Trubia M, Mancini M, Derme V, Nanni M, Lahortiga I, Riccioni R, Confalonieri S, Lo-Coco F, Di Fiore PP, Pelicci PG.

Genes Chromosomes Cancer. 2004 Nov;41(3):272-7.

PMID:
15334551
15.
16.

11q13 alterations in two cases of hibernoma: large heterozygous deletions and rearrangement breakpoints near GARP in 11q13.5.

Maire G, Forus A, Foa C, Bjerkehagen B, Mainguené C, Kresse SH, Myklebost O, Pedeutour F.

Genes Chromosomes Cancer. 2003 Aug;37(4):389-95.

PMID:
12800150
17.

Novel translocations that disrupt the platelet-derived growth factor receptor beta (PDGFRB) gene in BCR-ABL-negative chronic myeloproliferative disorders.

Baxter EJ, Kulkarni S, Vizmanos JL, Jaju R, Martinelli G, Testoni N, Hughes G, Salamanchuk Z, Calasanz MJ, Lahortiga I, Pocock CF, Dang R, Fidler C, Wainscoat JS, Boultwood J, Cross NC.

Br J Haematol. 2003 Jan;120(2):251-6.

PMID:
12542482
18.

Chromosomal alterations in small cell lung cancer revealed by multicolour fluorescence in situ hybridization.

Ashman JN, Brigham J, Cowen ME, Bahia H, Greenman J, Lind M, Cawkwell L.

Int J Cancer. 2002 Nov 20;102(3):230-6.

19.

H4(D10S170), a gene frequently rearranged in papillary thyroid carcinoma, is fused to the platelet-derived growth factor receptor beta gene in atypical chronic myeloid leukemia with t(5;10)(q33;q22).

Schwaller J, Anastasiadou E, Cain D, Kutok J, Wojiski S, Williams IR, LaStarza R, Crescenzi B, Sternberg DW, Andreasson P, Schiavo R, Siena S, Mecucci C, Gilliland DG.

Blood. 2001 Jun 15;97(12):3910-8.

20.
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