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Chromosomes in myelodysplastic syndrome: structural abnormalities of chromosome 11MUSILOVA, J; MICHALOVA, K; JAROSOVA, M et al.Annales de génétique (Paris). 1989, Vol 32, Num 1, pp 43-46, issn 0003-3995, 4 p.Article

Interstitial deletion of 11qGUC-SCEKIC, M; PILIC-RADIVOJEVIC, G; MRDJENOVIC, G et al.Journal of medical genetics. 1989, Vol 26, Num 3, pp 205-206, issn 0022-2593, 2 p.Article

Deficiency of all or part of chromosome 11 in several types of cancer: significance of a reduction in the number of normal chromosomes 11ATKIN, N. B; BAKER, M. C.Cytogenetics and cell genetics. 1988, Vol 47, Num 1-2, pp 106-107, issn 0301-0171Article

Allele loss on chromosome 11 in a pituitary tumor from a patient with multiple endocrine neoplasia type 1YOSHIMOTO, K; IWAHANA, H; KUBO, K et al.Japanese journal of cancer research. 1991, Vol 82, Num 8, pp 886-889, issn 0910-5050Article

11q23 involvement in a complex insertion (10;11) in acute monocytic leukemiaREGE-CAMBRIN, G; MECUCCI, C; VAN ORSHOVEN, A et al.Leukemia research. 1986, Vol 10, Num 9, pp 1159-1161, issn 0145-2126Article

Partial deletion 11q : report of a case with a large terminal deletion 11q21-qter without loss of telomeric sequences, and review of the literatureHERTZ, J. M; TOMMERUP, N; SØRENSEN, F. B et al.Clinical genetics. 1995, Vol 47, Num 5, pp 231-235, issn 0009-9163Article

Cytogenetic and molecular analysis of chromosome 11q23 abnormalities in leukaemiaYOUNG, B. D.Baillière's clinical haematology. 1992, Vol 5, Num 4, pp 881-895, issn 0950-3536Article

Preferential involvement of 11q23-24 and 11p15 in breast cancerFERTI-PASSANTONOPOULOU, A; PANANI, A. D; RAPTIS, S et al.Cancer genetics and cytogenetics. 1991, Vol 51, Num 2, pp 183-188, issn 0165-4608Article

Prenatal ultrasonographic findings associated with Jacobsen syndromeWAX, J. R; SMITH, J. F; FLOYD, R. C et al.Journal of ultrasound in medicine. 1995, Vol 14, Num 3, pp 256-258, issn 0278-4297Article

Trisomy 11 in nonlymphocytic neoplasiaOHYASHIKI, K; OHYASHIKI, J. H; IWABUCHI, A et al.British journal of haematology. 1988, Vol 69, Num 3, issn 0007-1048, 420Article

Intestitial deletion of the long arm of chromosome 11KLEP-DE PATER, J. M; DE FRANCE, H. F; BIJLSMA, J. B et al.Journal of medical genetics. 1985, Vol 22, Num 3, pp 224-226, issn 0022-2593Article

A terminal deletion of 11qSCHWARZ, C; MPOFU, C; WRAITH, J. E et al.Journal of medical genetics. 1992, Vol 29, Num 7, pp 511-512, issn 0022-2593Article

Deletion 11q23.3 without familial predispositionHAUSMANN, C; BACK, E; WOLFF, G et al.Human genetics. 1988, Vol 80, Num 2, issn 0340-6717, 205Article

Das klinische Erscheinungsbild der partiellen Monosomie von Chromosom 11 q = Aspects cliniques de la monosomie partielle du bras long du chromosome 11 = Clinical features of partial monosomy of chromosome 11qDÖRR, U.Monatsschrift für Kinderheilkunde. 1986, Vol 134, Num 11, pp 808-811, issn 0026-9298Article

NUP98-HOXD13 gene fusion in therapy-related acute myelogenous leukemiaRAZA-EGILMEZ, S. Z; JANI-SAIT, S. N; GROSSI, M et al.Cancer research (Baltimore). 1998, Vol 58, Num 19, pp 4269-4273, issn 0008-5472Article

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

Central nervous system abnormalities in chromosome delection at 11q23ONO, J; HARADA, K; HASEGAWA, T et al.Clinical genetics. 1994, Vol 45, Num 6, pp 325-329, issn 0009-9163Article

Monosomy 11q : report of two familial cases and review of the literatureHUSTINX, R; VERLOES, A; GRATTAGLIANO, B et al.American journal of medical genetics. 1993, Vol 47, Num 3, pp 312-317, issn 0148-7299Article

11q trisomy detected by fluorescence in situ hybridizationTAKANO, T; YAMANOUCHI, Y; KAWASHIMA, S et al.Clinical genetics. 1993, Vol 44, Num 6, pp 324-328, issn 0009-9163Article

Allelic loss from chromosome 11 in parathyroid tumorsFRIEDMAN, E; DE MARCO, L; GEJMAN, P. V et al.Cancer research (Baltimore). 1992, Vol 52, Num 24, pp 6804-6809, issn 0008-5472Article

Paracentric inversion 11q in Canadian HutteritesCHODIRKER, B. N; GREENBERG, C. R; PABELLO, P. D et al.Human genetics. 1992, Vol 89, Num 4, pp 450-452, issn 0340-6717Article

Translocation (11;22) in small cell osteosarcomaNOGUERA, R; NAVARRO, S; TRICHE, T. J et al.Cancer genetics and cytogenetics. 1990, Vol 45, Num 1, pp 121-124, issn 0165-4608, 4 p.Article

Loss of heterozygosity of markers on chromosome 11 in tumors from patients with multiple endocrine neoplasia syndrome type 1RADFORD, D. M; ASHLEY, S. W; WELLS, S. A et al.Cancer research (Baltimore). 1990, Vol 50, Num 20, pp 6529-6533, issn 0008-5472, 5 p.Article

Chromosomal rearrangement on chromosome 11q14-q21 in T cell acute lymphoblastic leukemiaBERGER, R; LE CONIAT, M; DERRE, J et al.Leukemia. 1989, Vol 3, Num 8, pp 560-562, issn 0887-6924Article

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