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THREE NEW SPECIES OF POUROUMA (CECROPIACEAE) OF THE GUIANA REGIONBERG CC; KOOY F.1982; BRITTONIA; ISSN 0007-196X; USA; DA. 1982; VOL. 34; NO 1; PP. 36-41Article

A human 12p-derived cosmid hybridizing to subsets of human and chimpanzee telomeresHÖGLUND, M; MITELMAN, F; MANDAHL, N et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 88-91, issn 0301-0171Conference Paper

Construction of Chinese hamster chromosome specific DNA libraries and their use in the analysis of spontaneous chromosome rearrangements in different cell linesBALAJEE, A. S; DOMINGUEZ, I; NATARAJAN, A. T et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 95-101, issn 0301-0171Conference Paper

Construction of a pulsed-field amp around D3S3 using partially demethylated DNAVAN DER HOUT, A. H; HULSBEEK, M. M. F; BUYS, C. H. C. M et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 134-137, issn 0301-0171Conference Paper

Additional assignment of the human 5S rRNA genes to chromosome region 1q31LOMHOLT, B; FREDERIKSEN, S; NEDERBY NIELSEN, J et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 76-79, issn 0301-0171Conference Paper

Chromosome banding patterns in the unisexual microteiid Gymnophthalmus underwoodi and in two related sibling species (Gumnophthalmidae, Sauria)YONENAGA-YASSUDA, Y; VANZOLINI, P. E; RODRIGUES, M. T et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 29-34, issn 0301-0171Conference Paper

Comparative mapping of the gene encoding the catalytic subunit of protein phosphatase type 1α(PPP1CA) to human, rat, and mouse chromosomesSAADAT, M; MIZUNO, Y; KIKUCHI, K et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 55-57, issn 0301-0171Conference Paper

Evolutionary conservation of a microsatellite in the Wilms Tumour (WT) gene : mapping in sheep and cattleVAIMAN, D; PAILHOUX, E; PAYEN, E et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 112-115, issn 0301-0171Conference Paper

Assignment of the human β-catenin gene (CTNNB1) to 3p22→p21.3 by fluorescence in situ hybridizationVAN HENGEL, J; NOLLET, F; BERX, G et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 68-70, issn 0301-0171Conference Paper

Human origin of micronuclei in human x hamster two-cell embryosTUSELL, L; ALVAREZ, R; GENESCA, A et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 41-44, issn 0301-0171Conference Paper

Regional localisation of 19 brain expressed sequence tags to human chromosome 11 using PCR amplification of somatic cell hybrid DNAsSLORACH, E. M; POLYMEROPOULOS, M. H; EVANS, K. L et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 71-75, issn 0301-0171Conference Paper

Regional localization of the ovine NRAMP gene to chromosome 2q41→q42 by in situ hybridizationPITEL, F; CRIBIU, E. P; YERLE, M et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 116-118, issn 0301-0171Conference Paper

The kinase insert domain receptor gene (KDR) has been relocated to chromosome 4q11→q12SAIT, S. N. J; DOUGHER-VERMAZEN, M; SHOWS, T. B et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 145-146, issn 0301-0171Conference Paper

The lymphoid proliferation-associated gene EPAG maps to human chromosome region Xq21→q22DIZIKES, G. J; BENNETT, J. S; METZ, R. J et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 126-128, issn 0301-0171Conference Paper

Two categories of synovial sarcoma defined by divergent chromosome translocation breakpoints in Xp11.2, with implications for the histologic sub-classification of synovial sarcomaRENWICK, P. J; REEVES, B. R; DAL CIN, P et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 58-63, issn 0301-0171Conference Paper

Second international workshop on human chromosome 13 mapping 1994SCHEFFER, H; KOOY, F; TE MEERMAN, G et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 1-22, issn 0301-0171Conference Proceedings

Germline mutation of microRNA-125a is associated with breast cancerLI, W; DUAN, R; KOOY, F et al.Journal of medical genetics. 2009, Vol 46, Num 5, pp 358-360, issn 0022-2593, 3 p.Article

The SOX8 gene is located within 700 kb of the tip of chromosome 16p and is deleted in a patient with ATR-16 syndromePFEIFER, D; POULAT, F; HOLINSKI-FEDER, E et al.Genomics (San Diego, Calif.). 2000, Vol 63, Num 1, pp 108-116, issn 0888-7543Article

Direct microdissection and microcloning of a translocation breakpoint region, t(1;11) (q42.2;q21), associated with schizophreniaMUIR, W. J; GOSDEN, C. M; PORTEOUS, D. J et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 35-40, issn 0301-0171Conference Paper

Dehydroepiandrosterone sulfotransferase gene (STD) : localization to human chromosome band 19q13.3OTTERNESS, D. M; MOHRENWEISER, H. W; BRANDRIFF, B. F et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 45-47, issn 0301-0171Conference Paper

Precise ordering of 26 cosmid markers on chromosome region 3p23→p21.3 by two-color FISH on human prophase chromosomes and stretched DNAsARIYAMA, T; KIMURA, T; YAMAKAWA, K et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 129-133, issn 0301-0171Conference Paper

Segregation analysis of four translocations, t(2;18), t(3;15), t(5;7), and t(10;12), by sperm chromosome studies and a review of the literatureESTOP, A. M; VAN KIRK, V; CIEPLY, K et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 80-87, issn 0301-0171Conference Paper

Selection of chromosome-specific primers and their use in simple and double PRINS techniques for rapid in situ identification of human chromosomesPELLESTOR, F; GIRARDET, A; LEFORT, G et al.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 138-142, issn 0301-0171Conference Paper

Three members of the human cystatin gene superfamily, AHSG, HRG, and KNG, map within one megabase of genomic DNA at 3q27RIZZU, P; BALDINI, A.Cytogenetics and cell genetics. 1995, Vol 70, Num 1-2, pp 26-28, issn 0301-0171Conference Paper

Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcomeVAN BON, B. W. M; MEFFORD, H. C; STEWART, H et al.Journal of medical genetics. 2009, Vol 46, Num 8, pp 511-523, issn 0022-2593, 13 p.Article

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