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

Human chromosome 11 DNA sequence and analysis including novel gene identificationTAYLOR, Todd D; NOGUCHI, Hideki; SHE, Xinwei et al.Nature (London). 2006, Vol 440, Num 7083, pp 497-500, issn 0028-0836, 4 p.Article

Subchromosomal assignment of the TSSC1 gene to human chromosome band 11p15.5 near the HBB gene clusterSCELFO, R; SABBIONI, S; BARBANTI-BRODANO, G et al.Cytogenetics and cell genetics. 1998, Vol 83, Num 1-2, pp 52-53, issn 0301-0171Article

RING 11 CHROMOSOME (46,XX,R11(P15Q25).VALENTE M; MULLER H; SPARKES RS et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 36; NO 3; PP. 345-350; BIBL. 12 REF.Article

partielle trisomie 11q23-q25. Neue Klinische Aspekte = Partial trisomy 11q23-q25. New clinical aspectsVON BRENNDORFF, A. Irtel; KROLL, M; DIETZ, I et al.Monatsschrift für Kinderheilkunde. 2002, Vol 150, Num 11, pp 1371-1377, issn 0026-9298, 7 p.Article

Anomalies of the long arm of chromosome 11 in human myelo- and lymphoproliferative disorders. I: Acute nonlymphocytic leukemia = Anomalies du bras long du chromosome 11 dans les affections myélo- et lymphoprolifératives. I. Leucémie aiguë non lymphoïdeVERMAELEN, K; BARBIERI, D; MICHAUX, J.-L et al.Cancer genetics and cytogenetics. 1983, Vol 10, Num 1, pp 105-116, issn 0165-4608Article

PARTIAL TRISOMY OF CHROMOSOME 11. A CASE REPORT = LA TRISOMIE PARTIELLE DU CHROMOSOME N^O11: UNE ETUDE DE CASFALK RE; CARREL RE; VALENTE M et al.1973; AMER. J. MENTAL DEFIC.; U.S.A.; DA. 1973; VOL. 77; NO 4; PP. 383-388; BIBL. 8REF.Serial Issue

Novel clinical features in a child with partial deletion of chromosome 11 [del(11)(q24.2)] : Further evidence for phenotypic heterogeneityGIAMPIETRO, Philip F; BABU, Deepti; ZABEL, Carrie A et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 4, pp 385-387, issn 1552-4825, 3 p.Article

Framework YAC contig anchored into a 3.2-Mb high-resolution physical map in proximal 11q13COURSEAUX, A; SZEPETOWSKI, P; GAUDRAY, P et al.Genomics (San Diego, Calif.). 1997, Vol 40, Num 1, pp 13-23, issn 0888-7543Article

Mapping FRA11A, a folate-sensitive fragile site in human chromosome band 11q13.3PERUCCA-LOSTANLEN, D; HECHT, B. K; COURSEAUX, A et al.Cytogenetics and cell genetics. 1997, Vol 79, Num 1-2, pp 88-91, issn 0301-0171Conference Paper

Assignment of human inhibitor of apoptosis protein (IAP) genes xiap, hiap-1, and hiap-2 to chromosomes Xq25 and 11q22-23 by fluorescencence in situ hybridizationRAJCAN-SEPAROVIC, E; LISTON, P; LEFEBVRE, C et al.Genomics (San Diego, Calif.). 1996, Vol 37, Num 3, pp 404-406, issn 0888-7543Article

Assignment of the human pyruvate carboxylase gene (PC) to 11q13.4 by fluorescence in situ hybridisationWALKER, M. E; BAKER, E; WALLACE, J. C et al.Cytogenetics and cell genetics. 1995, Vol 69, Num 3-4, pp 187-189, issn 0301-0171Article

Improving the comparative map of porcine chromosome 9 with respect to human chromosomes 1, 7 and 11MIDDLETON, R; ALDENHOVEN, J; CHEN, Y et al.Cytogenetic and genome research. 2003, Vol 102, Num 1-4, pp 128-132, issn 1424-8581, 5 p.Article

Comparative structure, proximal promoter elements, and chromosome location of the human eosinophil major basic protein genesPLAGER, Douglas A; WEILER, Deborah A; LOEGERING, David A et al.Genomics (San Diego, Calif.). 2001, Vol 71, Num 3, pp 271-281, issn 0888-7543Article

Chromosomal distribution, localization and expression of the human endogenous retrovirus ERV9SVENSSON, A-C; RAUDSEPP, T; LARSSON, C et al.Cytogenetics and cell genetics. 2001, Vol 92, Num 1-2, pp 89-96, issn 0301-0171Conference Paper

Assignment¹ of KPNA4 and KPNB1 encoding karyopherin alpha 4 and beta 1 to human chromosome bands 11q22 and 17q21 respectively, by in situ hybridizationAYALA-MADRIGAL, M. L; DOERR, S; RAMIREZ-DUENAS, M. L et al.Cytogenetics and cell genetics. 2000, Vol 89, Num 3-4, pp 258-259, issn 0301-0171Article

Tumorigenic conversion of immortal human skin keratinocytes (HaCaT) by elevated temperatureBOUKAMP, P; POPP, S; BLEUEL, K et al.Oncogene (Basingstoke). 1999, Vol 18, Num 41, pp 5638-5645, issn 0950-9232Article

Assignment of amyloid-precursor-like protein 2 gene (APLP2) to 11q24 by fluorescent in situ hybridizationLEACH, R; KO, M; KRAWETZ, S. A et al.Cytogenetics and cell genetics. 1999, Vol 87, Num 3-4, pp 215-216, issn 0301-0171Article

Report of the Sixth International Workshop on Human Chromosome 11 Mapping 1998GAUDRAY, P.Cytogenetics and cell genetics. 1999, Vol 86, Num 3-4, pp 167-186, issn 0301-0171Article

Genomic structure of uncoupling protein-3 (UCP3) and its assignment to chromosome 11q13BOSS, O; GIACOBINO, J.-P; MUZZIN, P et al.Genomics (San Diego, Calif.). 1998, Vol 47, Num 3, pp 425-426, issn 0888-7543Article

Detailed genetic mapping around a putative prostate-specific membrane antigen locus on human chromosome 11p11.2MARAJ, B. H; LEEK, J. P; KARAYI, M et al.Cytogenetics and cell genetics. 1998, Vol 81, Num 1, pp 3-9, issn 0301-0171Article

Assignment^a of the human TAF_II30 gene (TAF2H) to human chromosome band 11p15.3 using somatic cell hybridsCHDHENSSE, V; BOULVIN, C; LUCE, S et al.Cytogenetics and cell genetics. 1997, Vol 76, Num 1-2, pp 41-42, issn 0301-0171Article

Mapping of human non-muscle type cofilin (CFL1) to chromosome 11q13 and muscle-type cofilin (CFL2) to chromosome 14GILLETT, G. T; FOX, M. F; ROWE, P. S. N et al.Annals of human genetics. 1996, Vol 60, pp 201-211, issn 0003-4800, 3Article

The gene encoding the GPI-anchored membrane protein p137^GPI (M11S1) maps to human chromosome 11p13 and is highly conserved in the mouseGESSLER, M; KLAMT, B; TSAOUSSIDOU, S et al.Genomics (San Diego, Calif.). 1996, Vol 32, Num 1, pp 169-170, issn 0888-7543Article

Mapping of the metalloproteinase gene matrilysin (MMP7) to human chromosome 11q21→q22KNOX, J. D; BOREHAM, D. R; WALKER, J.-A et al.Cytogenetics and cell genetics. 1996, Vol 72, Num 2-3, pp 179-182, issn 0301-0171Conference Paper