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

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

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

Haplotype analysis of the apolipoprotein gene cluster on human chromosome 11OLIVIER, Michael; XUJING WANG; COLE, Regina et al.Genomics (San Diego, Calif.). 2004, Vol 83, Num 5, pp 912-923, issn 0888-7543, 12 p.Article

Interstitial deletion of chromosome 11 (q22.3-q23.2) in a boy with mild developmental delaySYRROU, M; FRYNS, J.-P.Journal of medical genetics. 2001, Vol 38, Num 9, pp 621-624, issn 0022-2593Article

Association between asthma and an intragenic variant of CC16 on chromosome 11q13MAO, X.-Q; SHIRAKAWA, T; KAWAI, M et al.Clinical genetics. 1998, Vol 53, Num 1, pp 54-56, issn 0009-9163Article

Identification and assignment of the human transient receptor potential channel 6 gene TRPC6 to chromosome 11q21→q22D'ESPOSITO, M; STRAZZULLO, M; CUCCURESE, M et al.Cytogenetics and cell genetics. 1998, Vol 83, Num 1-2, pp 46-47, issn 0301-0171Article

The high mobility group I-C gene (HMGI-C) : Polymorphism and genetic localizationISHWAD, C. S; SHRIVER, M. D; LASSIGE, D. M et al.Human genetics. 1997, Vol 99, Num 1, pp 103-105, issn 0340-6717Article

Assignment of the human gene for oct-binding factor-1 (OBF1), a B-cell-specific coactivator of octamer-binding transcription factors 1 and 2, to 11q23.1 by somatic cell hybridization and in situ hybridizationJUNKER, S; BRØNDUM-NIELSEN, K; NEWELL, J. W et al.Genomics (San Diego, Calif.). 1996, Vol 33, Num 1, pp 143-145, issn 0888-7543Article

Cloning of cDNA encoding human rapsyn and mapping of the RAPSN gene locus to chromosome 11p11.2-p11.1BUCKEL, A; BEESON, D; JAMES, M et al.Genomics (San Diego, Calif.). 1996, Vol 35, Num 3, pp 613-616, issn 0888-7543Article

Localization of the gene encoding the human L-glutamate transporter (GLT-1) to 11p11.2-p13 by fluorescence in situ hybridizationTAKAI, S; KAWAKAMI, H; NAKAYAMA, T et al.Human genetics. 1996, Vol 97, Num 3, pp 387-389, issn 0340-6717Article

Assignment of the human Integral TransMembrane protein 1 gene (ITM1) to human chromosome band 11q23.3 by in situ hybridisation and YAC mappingVAN HUL, W; HONG, G; WAUTERS, J et al.Cytogenetics and cell genetics. 1996, Vol 74, Num 3, pp 218-219, issn 0301-0171Conference Paper

Localization and physical mapping of the prostate-specific membrane antigen (PSM) gene to human chromosome 11RINKER-SCHAEFFER, C. W; HAWKINS, A. L; SU, S. L et al.Genomics (San Diego, Calif.). 1995, Vol 30, Num 1, pp 105-108, issn 0888-7543Article

Assignment of eight additional genes from human chromosome 11 to bovine chromosomes 15 and 29 : refinement of the comparative mapGAUTIER, M; HAYES, H; TAOURIT, S et al.Cytogenetics and cell genetics. 2001, Vol 93, Num 1-2, pp 60-64, issn 0301-0171Article

Linkage and association studies of atopy and the chromosome 11q13 regionDEICHMANN, K. A; STARKE, B; SCHLENTHER, S et al.Journal of medical genetics. 1999, Vol 36, Num 5, pp 379-382, issn 0022-2593Article

Assignment of the protein kinase homolog of YAK1 (HIPK3) to human chromosome band 11p13 by in situ hybridizationNUPPONEN, N. N; VISAKORPI, T.Cytogenetics and cell genetics. 1999, Vol 87, Num 1-2, pp 102-103, issn 0301-0171Article

A 5.5-Mb high-resolution integrated map of distal 11q13MERSCHER, S; BEKRI, S; DE LEEUW, B et al.Genomics (San Diego, Calif.). 1997, Vol 39, Num 3, pp 340-347, issn 0888-7543Article

Localization of genes encoding two human one-domain members of the AAA family : PSMC5 (the thyroid hormone receptor-interacting protein, TRIP1) and PSMC3 (the Tat-binding protein, TBP1)HOYLE, J; TAN, K. H; FISHER, E. M. C et al.Human genetics. 1997, Vol 99, Num 2, pp 285-288, issn 0340-6717Article

Linkage analysis between manic-depressive illness and markers on the long arm of chromosome 11EWALD, H; MORS, O; FLINT, T et al.American journal of medical genetics. 1995, Vol 60, Num 5, pp 386-392, issn 0148-7299Article