Human chromosome 7 circa 2004: a model for structural and functional studies of the human genomeSCHERER, Stephen W; GREEN, Eric D.Human molecular genetics (Print). 2004, Vol 13, pp R303-R313, issn 0964-6906, NS2Article

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

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

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

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

PARTIAL TRISOMY OF THE LONG ARM OF CHROMOSOME N^O7 = TRISOMIE PARTIELLE DU BRAS LONG DU CHROMOSOME N^O7ALFI OS; DONNELL GN; KRAMER SL et al.1973; J. MED. GENET.; G.B.; DA. 1973; VOL. 10; NO 2; PP. 187-189; BIBL. 4REF.Serial Issue

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

Assignment of cyclophilin A (PPIA) to human chromosome band 7p13 by in situ hybridizationBRAATEN, D; WELLINGTON, S; WARBURTON, D et al.Cytogenetics and cell genetics. 1996, Vol 74, Num 4, issn 0301-0171, p. 262Conference Paper

Recombinant Chromosome 7 in a Mosaic 45,X/47,XXX PatientTIRADO, Carlos A; GOTWAY, Garrett; KODURU, Prasad et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 1, pp 206-214, issn 1552-4825, 9 p.Article

Assignment¹ of the endogenous retrovirus HERV-R (ERV3) to human chromosome 7q11.2 by radiation hybrid mappingKIM, H.-S; CROW, T. J; HYUN, B.-H et al.Cytogenetics and cell genetics. 2000, Vol 89, Num 1-2, issn 0301-0171, p. 10Article

Mapping of the human cysteine-rich intestinal protein gene CRIP1 to the human chromosomal segment 7q11.23GARCIA-BARCELO, M; TSUI, S. K. W; CHIM, S. S et al.Genomics (San Diego, Calif.). 1998, Vol 47, Num 3, pp 419-422, issn 0888-7543Article

Assignment of the human podocalyxin-like protein (PODXL) gene to 7q32-q33KERSHAW, D. B; WIGGINS, J. E; WHARRAM, B. L et al.Genomics (San Diego, Calif.). 1997, Vol 45, Num 1, pp 239-240, issn 0888-7543Article

Physical mapping of the HOXA1 gene and the hnRPA2B1 gene in a YAC contig from human chromosome 7p14-p15VAN LAER, L; VAN CAMP, G; GREEN, E. D et al.Human genetics. 1997, Vol 99, Num 6, pp 831-833, issn 0340-6717Article

Genomic organization of the human endogenous retrovirus HERV-K(HML-2.HOM) (ERVK6) on chromosome 7REUS, Katrin; MAYER, Jens; SAUTER, Marlies et al.Genomics (San Diego, Calif.). 2001, Vol 72, Num 3, pp 314-320, issn 0888-7543Article

High-resolution detection of loss of heterozygosity of dinucleotide microsatellite markersHOURIHAN, Rebecca N; O'SULLIVAN, Gerald C; MORGAN, John G et al.BioTechniques. 2001, Vol 30, Num 2, pp 342-346, issn 0736-6205, 4 p.Article

Assignment of the human CC chemokine MPIF-2/eotaxin-2 (SCYA24) to chromosome 7q11.23NOMIYAMA, H; OSBORNE, L. R; IMAI, T et al.Genomics (San Diego, Calif.). 1998, Vol 49, Num 2, pp 339-340, issn 0888-7543Article

Mapping of the human lunatic fringe (LFNG) gene to 7p22 and manic fringe (MFNG) to 22q12EGAN, S; HERBRICK, J.-A; TSUI, L.-C et al.Genomics (San Diego, Calif.). 1998, Vol 54, Num 3, pp 576-577, issn 0888-7543Article

Six new polymorphic microsatellite markers used for the integration of genetic and physical maps of human chromosome 7BECK, S; BADBANCHI, F; OTTO, M et al.Human genetics. 1996, Vol 97, Num 6, pp 842-844, issn 0340-6717Article

Use of chromosome engineering to model a segmental deletion of chromosome band 7q22 found in myeloid malignanciesWONG, Jasmine C. Y; YAN ZHANG; LE BEAU, Michelle M et al.Blood. 2010, Vol 115, Num 22, pp 4524-4532, issn 0006-4971, 9 p.Article