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Localization¹ of the human anterior gradient-2 gene (AGR2) to chromosome band 7p21.3 by radiation hybrid mapping and fluorescence in situ hybridisationPETEK, E; WINDPASSINGER, C; EGGER, H et al.Cytogenetics and cell genetics. 2000, Vol 89, Num 3-4, pp 141-142, issn 0301-0171Article

Two RFLPs identified by an anonymous sequence (D7S19) (pTS119) from chromosome 7STARR, T; WOOD, S; RIDDELL, D. C et al.Nucleic acids research. 1987, Vol 15, Num 6, issn 0305-1048, 2784Article

Linkage between the cystic fibrosis locus and markers on chromosome 7qWAINWRIGHT, B; SCAMBLER, P; FARRALL, M et al.Cytogenetics and cell genetics. 1986, Vol 41, Num 3, pp 191-192, issn 0301-0171Article

Assignment of the human homologue of the Drosophila cut homoebox gene (CUTL1) to band 7q22 by fluorescence in situ hybridizationLEMIEUX, N; XIAO-XIANG ZHANG; DUFORT, D et al.Genomics (San Diego, Calif.). 1994, Vol 24, Num 1, pp 191-193, issn 0888-7543Article

A craniosynostosis in a boy with a del(7)(p15.3p21.3): assignment by deletion mapping of the critical segment for craniosynostosis to the mid-portion of 7p21MOTEGI, T; OHUCHI, M; OHTAKI, C et al.Human genetics. 1985, Vol 71, Num 2, pp 160-162, issn 0340-6717Article

Gene dosage studies regionally assign the phosphoserine phosphatase gene to 7p 15.1 or 2NOVELLI, G; DALLAPICCOLA, B.Annales de génétique (Paris). 1988, Vol 31, Num 3, pp 195-196, issn 0003-3995Article

Isolation of the human MOX2 homeobox gene and localization to chromosome 7p22.1-p21.3GRIGORIOU, M; KASTRINAKI, M.-C; MODI, W. S et al.Genomics (San Diego, Calif.). 1995, Vol 26, Num 3, pp 550-555, issn 0888-7543Article

Genetic linkage map of human chromosome 7 with 63 DNA markersBARKER, D; GREEN, P; HELMS, C et al.Proceedings of the National Academy of Sciences of the United States of America. 1987, Vol 84, Num 22, pp 8006-8010, issn 0027-8424Article

Genetic Mapping of Glutaric Aciduria, Type 3, to Chromosome 7 and Identification of Mutations in C7orf10SHERMAN, Eric A; STRAUSS, Kevin A; TORTORELLI, Silvia et al.American journal of human genetics. 2008, Vol 83, Num 5, pp 604-609, issn 0002-9297, 6 p.Article

Chromosomal localization of two kox zinc finger genes on chromosome bands 7q21-q22ROUSSEAU-MERCK, M.-F; DURO, D; BERGER, R et al.Annales de génétique (Paris). 1995, Vol 38, Num 2, pp 81-84, issn 0003-3995Article

Mapping of the human Zn-α₂-glycoprotein gene (AZGP1) to chromosome 7q22 by in situ hybridizationPENDAS, A. M; MATILLA, T; URIA, J. A et al.Cytogenetics and cell genetics. 1994, Vol 66, Num 4, pp 263-266, issn 0301-0171Conference Paper

Chromosomal mapping of the metastasis associated MTS1 gene by in situ hybridizationLAKSHMI, M. S; PARKER, C; SHERBET, G. V et al.Cytologia. 1992, Vol 57, Num 2, pp 273-276, issn 0011-4545Article

Interleukin 4 is at 5q31 and interleukin 6 is at 7p15SUTHERLAND, G. R; BAKER, E; VADAS, M. A et al.Human genetics. 1988, Vol 79, Num 4, pp 335-337, issn 0340-6717Article

Linkage of cystic fibrosis to the proα2(I) collagen gene, COL1A2, on chromosome 7BUCHWALD, M; ZSIGA, M; TSUI, L.-C et al.Cytogenetics and cell genetics. 1986, Vol 41, Num 4, pp 234-239, issn 0301-0171Article

Assignment of the human ADP-ribosylation factor 6 (ARF6) gene to chromosome 7q22.1 by radiation hybrid mappingKIM, H.-S.Cytogenetics and cell genetics. 1999, Vol 84, Num 1-2, issn 0301-0171, p. 94Article

Subregional localization of 21 chromosome 7-specific expressed sequence tags (ESTs) by FISH using newly identified YACs and P1sMORTON, S. M; VEILE, R. A; HELMS, C et al.Genomics (San Diego, Calif.). 1997, Vol 46, Num 3, pp 491-494, issn 0888-7543Article

Assignment of the 5-hydroxytryptamine (serotonin) receptor 5A gene (HTR5A) to human chromosome band 7q36.1SCHANEN, N. C; SCHERER, S. W; TSUI, L.-C et al.Cytogenetics and cell genetics. 1996, Vol 72, Num 2-3, pp 187-188, issn 0301-0171Conference Paper

Localization of the human OB gene (OBS) to chromosome 7q32 by fluorescence in situ hybridizationGEFFROY, S; DE VOS, P; STAELS, B et al.Genomics (San Diego, Calif.). 1995, Vol 28, Num 3, pp 603-604, issn 0888-7543Article

Sacral dysgenesis associated with terminal deletion of chromosome 7q : a report of two familiesWANG, J; SPITZ, L; REARDON, W et al.European journal of pediatrics. 1999, Vol 158, Num 11, pp 902-905, issn 0340-6199Article

Familial reciprocal translocation t(7;16) associated with maternal uniparental disomy 7 in a Silver-Russell patientDUPONT, Jean-Michel; CUISSET, Laurence; CARTIGNY, Maryse et al.American journal of medical genetics. 2002, Vol 111, Num 4, pp 405-408, issn 0148-7299Article

Occurrence of Cancer in a cohort of 183 persons with constitutional chromosome 7 abnormalitiesHASLE, H; OLSEN, J. H; HANSEN, J et al.Cancer genetics and cytogenetics. 1998, Vol 105, Num 1, pp 39-42, issn 0165-4608Article

Novel CUX1 missense mutation in association with 7q― at leukemic transformation of MPNTHOENNISSEN, Nils H; LASHO, Terra; THOENNISSEN, Gabriela B et al.American journal of hematology. 2011, Vol 86, Num 8, pp 703-705, issn 0361-8609, 3 p.Article

Chromosomal localization of the human and murine orthologues of the Drosophila smoothened geneCHIDAMBARAM, A; GERRARD, B; HANSON, M et al.Genomics (San Diego, Calif.). 1998, Vol 53, Num 3, pp 416-417, issn 0888-7543Article

Further delineation of 7p trisomy : Case report and review literaturePALLOTTA, R; DALPRA, L; FUSILLI, P et al.Annales de génétique (Paris). 1996, Vol 39, Num 3, pp 152-158, issn 0003-3995Article