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At least nine cases of trisomy 11q23→qter in one generation as a result of familial t(11;13) translocationSMEETS, D; VAN RAVENSWAAIJ, C; DE PATER, J et al.Journal of medical genetics. 1997, Vol 34, Num 1, pp 18-23, issn 0022-2593Article

Interstitial deletion 11q. Case report and review of the literatureDE PATER, J. M; IPPEL, P. F; BIJLSMA, J. B et al.Genetic counseling. 1997, Vol 8, Num 4, pp 335-339, issn 1015-8146Conference Paper

Loss of heterozygosity and heterogeneity of its appearance and persisting in the course of acute myeloid leukemia and myelodysplastic syndromesKRSKOVA-HONZATKOVA, Lenka; CERMAK, Jaroslav; SAJDOVA, Jana et al.Leukemia research. 2001, Vol 25, Num 1, pp 45-53, issn 0145-2126Article

Prenatal diagnosis of a De Novo ring chromosome 11MOHAMED, Anwar N; EBRAHIM, Salah A; AATRE, Rajani et al.American journal of medical genetics. 2001, Vol 102, Num 4, pp 368-371, issn 0148-7299Article

Occurence of a novel t(11;19)(q13;q13.3) in complete remission of acute promyelocytic leukemiaTEMPERANI, P; LUPPI, M; GIACOBBI, F et al.Cancer genetics and cytogenetics. 1998, Vol 101, Num 1, pp 35-38, issn 0165-4608Article

EMS1 amplification can occur independently of CCND1 or INT-2 amplification at 11q13 and may identify different phenotypes in primary breast cancerHUI, R; CAMPBELL, D. H; LEE, C. S. L et al.Oncogene (Basingstoke). 1997, Vol 15, Num 13, pp 1617-1623, issn 0950-9232Article

Unbalanced t(4;11)(q32;q23) in a 34-year-old man with manifestations of distal monosomy 11q and trisomy 4q syndromesBYATT, S.-A; BAKER, E; RICHARDS, R. I et al.American journal of medical genetics. 1997, Vol 70, Num 4, pp 357-360, issn 0148-7299Article

Deletions at 11q identify a subset of patients with typical CLL who show consistent disease progression and reduced survivalNEILSON, J. R; AUER, R; WHITE, D et al.Leukemia. 1997, Vol 11, Num 11, pp 1929-1932, issn 0887-6924Article

Partial deletion of the long arm of chromosome 11 : ten Japanese childrenONO, J; HASEGAWA, T; OKADA, S et al.Clinical genetics. 1996, Vol 50, Num 6, pp 474-478, issn 0009-9163Article

Chromosome 11 abnormalities in myelodysplastic syndromesCOLLADO, R; BADIA, L; GARCIA, S et al.Cancer genetics and cytogenetics. 1999, Vol 114, Num 1, pp 58-61, issn 0165-4608Article

Detection of structural abnormalities in spermatozoa of a translocation carrier t(3;11)(q27.3;q24.3) by triple FISHMARTINI, E; VON BERGH, A. R. M; COONEN, E et al.Human genetics. 1998, Vol 102, Num 2, pp 157-165, issn 0340-6717Article

Reciprocal translocation 4;11 with both adjacent-1 segregants viable within a familyCELLARS ROGERS, J; HARRIS, D. J; PASZTOR, L. M et al.Clinical genetics. 1997, Vol 51, Num 4, pp 250-256, issn 0009-9163Article

Molecular analysis of t(11;19) breakpoints in childhood acute leukemiasRUBNITZ, J. E; BEHM, F. G; CURCIO-BRINT, A. M et al.Blood. 1996, Vol 87, Num 11, pp 4804-4808, issn 0006-4971Article

Interstitial deletion of 11(p11.2p12) : A newly described contiguous gene deletion syndrome involving the gene for hereditary multiple exostoses (EXT2)POTOCKI, L; SHAFFER, L. G.American journal of medical genetics. 1996, Vol 62, Num 3, pp 319-325, issn 0148-7299Conference Paper

Karyotypic evolution in CLL : identification of a new sub-group of patients with deletions of 11q and advanced or progressive diseaseFEGAN, C; ROBINSON, H; THOMPSON, P et al.Leukemia. 1995, Vol 9, Num 12, pp 2003-2008, issn 0887-6924Article

Novel non-TCR chromosome translocations t(3;11)(q25;p13) and t(X;11)(q25;p13) activating LMO2 by juxtaposition with MBNL1 and STAG2CHEN, S; NAGEL, S; SCHNEIDER, B et al.Leukemia. 2011, Vol 25, Num 10, pp 1632-1635, issn 0887-6924, 4 p.Article

Asplenia syndrome in a child with a balanced reciprocal translocation of chromosomes 11 and 20 [46,XX,t(11;20)(q13.1;q13.13)]FREEMAN, S. B; KASINATHAN MURALIDHARAN; PETTAY, D et al.American journal of medical genetics. 1996, Vol 61, Num 4, pp 340-344, issn 0148-7299Article

Chromosome 11 abnormalities in Bowen disease of the vulvaSWANSON, G. P; DOBIN, S. M; ARBER, J. M et al.Cancer genetics and cytogenetics. 1997, Vol 93, Num 2, pp 109-114, issn 0165-4608Article

Familial Wolf-Hirshhorn syndrome resulting from a cryptic translocation : a clinical and molecular studyREID, E; MORRISON, N; BARRON, L et al.Journal of medical genetics. 1996, Vol 33, Num 3, pp 197-202, issn 0022-2593Article

Poor prognosis in multiple myeloma is associated only with partial or complete deletions of chromosome 13 or abnormalities involving 11q and not with other karyotype abnormalitiesTRICOT, G; BARLOGIE, B; SUNDAR JAGANNATH et al.Blood. 1995, Vol 86, Num 11, pp 4250-4256, issn 0006-4971Article

Jumping translocations involving 11q in a non-hodgkin lymphomaPETKOVIC, I; KONJA, J; DOMINIS, M et al.Cancer genetics and cytogenetics. 1999, Vol 114, Num 2, pp 121-125, issn 0165-4608Article

Novel transcribed sequences neighbouring a translocation breakpoint associated with schizophreniaDEVON, R. S; EVANS, K. L; MAULE, J. C et al.American journal of medical genetics. 1997, Vol 74, Num 1, pp 82-90, issn 0148-7299Article

Cyclin D1 gene amplification in human laryngeal squamous cell carcinomas : prognostic significance and clinical implicationsBELLACOSA, A; ALMADORI, G; CAVALLO, S et al.Clinical cancer research. 1996, Vol 2, Num 1, pp 175-180, issn 1078-0432Article

Jacobsen syndrome : report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11(q23q25) and review of 52 casesPIVNICK, E. K; VELAGALETI, G. V. N; WILROY, R. S et al.Journal of medical genetics. 1996, Vol 33, Num 9, pp 772-778, issn 0022-2593Article