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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

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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

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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

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Loss of heterozygosity on chromosome 11q13 in microdissected human male breast carcinomasSANZ-ORTEGA, J; CHUAQUI, R; ZHENGPING ZHUANG et al.Journal of the National Cancer Institute. 1995, Vol 87, Num 18, pp 1408-1410, issn 0027-8874Article

Mixed phenotype acute leukemia with t(11;19)(q23;p13.3)/ MLL-MLLT1 (ENL), B/T-lymphoid type: A first case reportNAGHASHPOUR, Mojdeh; LANCET, Jeffrey; MOSCINSKI, Lynn et al.American journal of hematology. 2010, Vol 85, Num 6, pp 451-454, issn 0361-8609, 4 p.Article

Strikingly different molecular relapse kinetics in NPM1c, PML-RARA, RUNX1-RUNX1T1, and CBFB-MYH11 acute myeloid leukemiasOMMEN, Hans Beier; SCHNITTGER, Susanne; JOVANOVIC, Jelena V et al.Blood. 2010, Vol 115, Num 2, pp 198-205, issn 0006-4971, 8 p.Article

t(3;11)(q12;p15)/NUP98-LOC348801 fusion transcript in acute myeloid leukemiaGORELLO, Paolo; BRANDIMARTE, Lucia; LA STARZA, Roberta et al.Haematologica (Roma). 2008, Vol 93, Num 9, pp 1398-1401, issn 0390-6078, 4 p.Article

Paris-Trousseau syndrome: clinical, hematological, molecular data of ten new casesFAVIER, Remi; JONDEAU, Katayoun; BOUTARD, Patrice et al.Thrombosis and haemostasis. 2003, Vol 90, Num 5, pp 893-897, issn 0340-6245, 5 p.Article

Variant translocations of 11q23 in infant acute lymphoblastic leukemia (ALL): Do outcomes differ from t(4;11)?JAKAB, Zsuzsanna; BALOGH, Erzsébet; KARASZI, Eva et al.Medical and pediatric oncology. 2002, Vol 39, Num 1, pp 63-65, issn 0098-1532Article

Prognostic significance of molecular genetic aberrations on chromosome segment 11p15.5 in non-small-cell lung cancerBEPLER, Gerold; GAUTAM, Ashish; MCINTYRE, Lauren M et al.Journal of clinical oncology. 2002, Vol 20, Num 5, pp 1353-1360, issn 0732-183XArticle

Deletion mapping of chromosome segment 11Q24-q25, exhibiting extensive allelic loss in early onset breast cancerGENTILE, Massimilano; WIMAN, Asa; THORSTENSON, Sten et al.International journal of cancer. 2001, Vol 92, Num 2, pp 208-213, issn 0020-7136Article

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T-cell prolymphocytic leukemia with a novel translocation (6;11)(q21;q23)WONG, K. F; CHAN, J. K. C; SIN, V. C et al.Cancer genetics and cytogenetics. 1999, Vol 111, Num 2, pp 149-151, issn 0165-4608Article