Mapping of the gene for multiple endocrine neoplasia type I to chromosone 11q13NORDENSKJOLD, M; LARSSON, C; OBERG, K et al.Transactions of the Zoological Society of London. 1989, Vol 37, Num 9, issn 0084-5620, 951 [1 p.]Conference Paper

A gene specifying subunit VIII of human cytochrome c oxidase is localized to chromosome 11 and is expressed in both muscle and non-muscle tissuesRIZZUTO, R; NAKASE, H; DARRAS, B et al.The Journal of biological chemistry (Print). 1989, Vol 264, Num 18, pp 10595-10600, issn 0021-9258, 6 p.Article

Chromasome deletion at 11q23 in an abnormal child from a family with inherited fragility at 11q23VOULLAIRE, L. E; WEBB, G. C; LEVERSHA, M. A et al.Human genetics. 1987, Vol 76, Num 2, pp 202-204, issn 0340-6717Article

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

High-resolution physical mapping of a 250-kb region of human chromosome 11q24 by genomic sequence sampling (GSS)SELLERI, L; SMITH, M. W; HOLMSEN, A. L et al.Genomics (San Diego, Calif.). 1995, Vol 26, Num 3, pp 489-501, issn 0888-7543Article

Mapping of ribosomal protein S3 and internally nested snoRNA U15A gene to human chromosome 11q13.3-q13.5POLAKIEWICZ, R. D; MUNROE, D. J; JANI SAIT, S. N et al.Genomics (San Diego, Calif.). 1995, Vol 25, Num 2, pp 577-580, issn 0888-7543Article

Mapping of 28 (CA)_n microsatellite repeats and 13 Alu markers on human chromosome 11 using a panel of somatic cell hybridsIIZUKA, M; JONES, C; HAYASHI, K et al.Genomics (San Diego, Calif.). 1994, Vol 19, Num 3, pp 581-584, issn 0888-7543Article

Localization of the human CD59 gene by fluorescence in situ hybridization and pulsed-field gel electrophoresisHECKL-ÖSTREICHER, B; RAGG, S; DRECHSLER, M et al.Cytogenetics and cell genetics. 1993, Vol 63, Num 3, pp 144-146, issn 0301-0171Article

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

A third human CALC (pseudo)gene on chromosome 11HOPPENER, J. W. M; STEENBERGH, P. H; ZANDBERG, J et al.FEBS letters. 1988, Vol 233, Num 1, pp 57-63, issn 0014-5793Article

Assignment of the structural gene for subunit M1 of human ribonucleotide reductase to the short arm of chromosome 11ENGSTROM, Y; FRANCKE, U.Experimental cell research. 1985, Vol 158, Num 2, pp 477-483, issn 0014-4827Article

Assignment of the gene SLC1A2 coding for the human glutamate transporter EAAT2 to human chromosome 11 bands p13-p12LI, X; FRANCKE, U.Cytogenetics and cell genetics. 1995, Vol 71, Num 3, pp 212-213, issn 0301-0171Article

Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1 : evidence for genetic heterogeneityMARIMAN, E. C. M; VAN BEERSUM, S. E. C; CREMERS, C. W. R. J et al.Human genetics. 1995, Vol 95, Num 1, pp 56-62, issn 0340-6717Article

Factors confounding genetic linkage between atopy and chromosome 11qMOFFATT, M. F; SHARP, P. A; FAUX, J. A et al.Clinical and experimental allergy (Print). 1992, Vol 22, Num 12, pp 1046-1051, issn 0954-7894Article

Localization of an ataxia-telangiectasia locus to a 3-cM interval on chromosome 11q23 : linkage analysis of III families by an international consortiumFOROUD, T; WEI, S; CHARMLEY, P et al.American journal of human genetics. 1991, Vol 49, Num 6, pp 1263-1279, issn 0002-9297Article

Isolation and mapping of a polymorphic DNA sequence MCT128.1 on chromosome 11 [D11S285]CARLSON, M; NAKAMURA, Y; KRAPCHO, K et al.Nucleic acids research. 1988, Vol 16, Num 1, issn 0305-1048, 378Article

Isolation and mapping of a polymorphic DNA sequence pHBI18P2 on chromosome 11 [D11S147]NAKAMURA, Y; GILLILAN, S; O'CONNELL, P et al.Nucleic acids research. 1988, Vol 16, Num 1, issn 0305-1048, 377Article

An ecoRI polymorphism associated with a human genomic clone from band 11p13HUFF, V; COMPTON, D; LEWIS, W et al.Nucleic acids research. 1987, Vol 15, Num 18, issn 0305-1048, 7651Article

Assignment of the human ribosomal protein S25 gene (RPS25) to chromosome 11q23.3 by sequence analysis of the marker D11456IMAI, T; SUDO, K; MIWA, T et al.Genomics (San Diego, Calif.). 1994, Vol 20, Num 1, pp 142-143, issn 0888-7543Article

Dinucleotide repeat polymorphism at 11q23TELATAR, M; CONCANNON, P; TOLUN, A et al.Human genetics. 1994, Vol 94, Num 1, issn 0340-6717, p. 109Article

Assignment of the β-arrestin 1 gene (ARRB1) to human chromosome 11q13CALABRESE, G; SALLESE, M; STORNAIUOLO, A et al.Genomics (San Diego, Calif.). 1994, Vol 24, Num 1, pp 169-171, issn 0888-7543Article

Dinucleotide repeat polymorphism at the D11S995 locusBROWNE, D. L; VAN HEYNINGEN, V; BICKMORE, W et al.Human molecular genetics (Print). 1993, Vol 2, Num 8, issn 0964-6906, p. 1332Article

Midkine gene (MDK), a gene for prenatal differentiation and neuroregulation, maps to band 11p11.2 by fluorescence in situ hybridizationKANAME, T; KUWANO, A; MURANO, I et al.Genomics (San Diego, Calif.). 1993, Vol 17, Num 2, pp 514-515, issn 0888-7543Article

Mapping of 262 DNA markers into 24 intervals on human chromosome IITANIGAMI, A; TOKINO, T; TAKIGUCHI, S et al.American journal of human genetics. 1992, Vol 50, Num 1, pp 56-64, issn 0002-9297Article