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Results 1 to 25 of 2199

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A centromere-based linkage group on the long arm of human chromosome 17TSIPOURAS, P; SCHWARTZ, R. C; PHILLIPS, J. A. III et al.Cytogenetics and cell genetics. 1988, Vol 47, Num 1-2, pp 109-110, issn 0301-0171Article

A moderately frequent RFLP identified by both SacI and BanII with a probe from the HOX2 locus in man (17q11-17q22)MURPHY, P. D; FERGUSON-SMITH, A. C; MIKI, T et al.Nucleic acids research. 1987, Vol 15, Num 15, issn 0305-1048, 6311Article

The gene cluster for human U2 RNA is located on chromosome 17q21HAMMARSTROM, K; SANTESSON, B; WESTIN, G et al.Experimental cell research. 1985, Vol 159, Num 2, pp 473-478, issn 0014-4827Article

Assignment of human platelet GP2B (GPIIb) gene to chomosome 17, region q21.1-q21.3NGUYEN VAN CONG; UZAN, G; GROSS, M. S et al.Human genetics. 1988, Vol 80, Num 4, pp 389-392, issn 0340-6717Article

Human p53 gene localized to short arm of chromosome 17MILLER, C; MOHANDAS, T; WOLF, D et al.Nature (London). 1986, Vol 319, Num 6056, pp 783-784, issn 0028-0836Article

DUPLICATION (PARTIAL TRISOMY) OF THE DISTAL LONG ARM OF CHROMOSOME 17: A NEW CLINICALLY RECOGNIZABLE CHROMOSOME DISORDERBERBERICH MS; CAREY JC; LAWCE HJ et al.1978; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1978; VOL. 14; NO 6C; PP. 287-295; BIBL. 3 REF.Article

Assignment of the acute phase response factor (APRF) gene to 17q21 by microdissection clone sequencing and fluorescence in situ hybridization of a P1 cloneCHOI, J. Y; WAN LIANG LI; KOURI, R. E et al.Genomics (San Diego, Calif.). 1996, Vol 37, Num 2, pp 264-265, issn 0888-7543Article

The human cytochrome b561 gene (CYB561) is located at 17q11-qterMCBRIDE, O. W; HUA FANG YI; SRIVASTAVA, M et al.Genomics (San Diego, Calif.). 1994, Vol 21, Num 3, pp 662-663, issn 0888-7543Article

Localization of glucose-dependent insulinotropic polypeptide (GIP) to a gene cluster on chromosome 17qLEWIS, T. B; SAENZ, M; O'CONNELL, P et al.Genomics (San Diego, Calif.). 1994, Vol 19, Num 3, pp 589-591, issn 0888-7543Article

CRK proto-oncogene maps to human chromosome band 17p13FIORETOS, J; HEISTERKAMP, N; GROFFEN, J et al.Oncogene (Basingstoke). 1993, Vol 8, Num 10, pp 2853-2855, issn 0950-9232Article

The case of the gray optic disc!BRODSKY, M. C; BUCKLEY, E. G; MCCONKIE-ROSELL, A et al.Survey of ophthalmology. 1989, Vol 33, Num 5, pp 367-372, issn 0039-6257Article

Random cloning of genes from mouse chromosome 17KASAHARA, M; FIGUEROA, F; KLEIN, J et al.Proceedings of the National Academy of Sciences of the United States of America. 1987, Vol 84, Num 10, pp 3325-3328, issn 0027-8424Article

CYTOCHEMICAL ANALYSIS ON A CASE OF FAMILIAL 17 PSAU W; WITEK JA.1979; HUM. GENET.; DEU; DA. 1979; VOL. 48; NO 2; PP. 195-199; BIBL. 19 REF.Article

A (9; 17) TRANSLOCATION, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. 6M-988.LIN CC; KAVANAGH AJ; ARONSON MM et al.1977; CYTOGENET. CELL GENET.; SWITZ.; DA. 1977; VOL. 18; NO 4; PP. 244Article

Physical mapping of chromosome 17 cosmids by fluorescence in sity hybridization and digital image analysisKALLIONIEMI, O.-P; KALLIONIEMI, A; MASCIO, L et al.Genomics (San Diego, Calif.). 1994, Vol 20, Num 1, pp 125-128, issn 0888-7543Article

A sequence-ready map of the human chromosome 17p telomereXIANG, Z; HU, X.-L; FLINT, J et al.Genomics (San Diego, Calif.). 1999, Vol 58, Num 2, pp 207-210, issn 0888-7543Article

Assignmenta of the human 14-3-3 epsilon isoform (YWHAE) to human chromosome 17p13 by in situ hybridizationLUK, S. C. W; GARCIA-BARCELO, M; TSUI, S. K. W et al.Cytogenetics and cell genetics. 1997, Vol 78, Num 2, pp 105-106, issn 0301-0171Article

Assignement of apolipoprotein H (APOH: beta-2-glycoprotein I) to human chromosome 17q23→qter; determination of the major expression siteSTEINKASSERER, A; COCKBURN, D. J; BLACK, D. M et al.Cytogenetics and cell genetics. 1992, Vol 60, Num 1, pp 31-33, issn 0301-0171Article

THE SAME MARKER CHROMOSOME, MAR 17P+, IN FOUR CONSECUTIVE CASES OF MULTIPLE MYELOMAMANOLOVA Y; MANOLOV G; APOSTOLOV P et al.1979; HEREDITAS; SWE; DA. 1979; VOL. 90; NO 2; PP. 307-310; BIBL. 9 REF.Article

ISOCHROMOSOME 17 IN ATYPICAL MYELOPROLIFERATIVE AND LYMPHOPROLIFERATIVE DISORDERS.NOWELL PC; FINAN JB.1977; J. NATION. CANCER INST.; U.S.A.; DA. 1977; VOL. 59; NO 2; PP. 329-333; BIBL. 23 REF.Article

AN AUTOPSY CASE OF PRIMARY ACQUIRED SIDEROBLASTIC ANEMIA XITH ISOCHROMOSOME 17 ABERRATION.HATTA Y; OKUMURA Y; NARAMOTO C et al.1976; JAP. J. MED.; JAP.; DA. 1976; VOL. 15; NO 2; PP. 139-145; BIBL. 26 REF.Article

PURE TRISOMY 17P IN 60% OF CELLSSHABTAI F; SHALEV A; CHEMKE J et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 52; NO 3; PP. 263-268; BIBL. 12 REF.Article

Human artificial chromosomes containing chromosome 17 alphoid DNA maintain an active centromere in murine cells but are not stableALAZAMI, Anas M; MEJIA, José E; MONACO, Zoia Larin et al.Genomics (San Diego, Calif.). 2004, Vol 83, Num 5, pp 844-851, issn 0888-7543, 8 p.Article

Hemizygosity for the COP9 signalosome subunit gene, SGN3, in the Smith-Magenis syndromeELSEA, S. H; MYKYTYN, K; FERRELL, K et al.American journal of medical genetics. 1999, Vol 87, Num 4, pp 342-348, issn 0148-7299Article

Assignment of the human phosphoribosylpyrophosphate synthetase-associated protein 41 gene (PRPSAP2) to 17p11.2-p12KATASHIMA, R; IWAHANA, H; FUJIMURA, M et al.Genomics (San Diego, Calif.). 1998, Vol 54, Num 1, pp 180-181, issn 0888-7543Article

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