Works matching IS 03010171 AND DT 1998 AND VI 81 AND IP 3/4
Results: 36
Report of the Fourth International Workshop on Human Chromosome 5 mapping 1996.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 169, doi. 10.1159/000015019
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Assignment[sup 1] of the hepatocyte nuclear factor 3 genes to rat chromosome bands 6q23→q24 (alpha: Hnf3a ), 3q41 (beta: Hnf3b ) and 1q21→q22 (gamma: Hnf3g ) by in situ hybridization.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 174, doi. 10.1159/000015020
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Assignment[sup 1] of AR1, transcription factor 20 (TCF20), to human chromosome 22q13.3 with somatic cell hybrids and in situ hybridization.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 176, doi. 10.1159/000015021
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Assignment[sup 1] of a human putative RNA helicase gene, DDX3, to human X chromosome bands p11.3→p11.23.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 178, doi. 10.1159/000015022
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Assignment[sup 1] of H7365 (C9orf2) to human chromosome band 9q31 by somatic cell hybrid analysis and fluorescence in situ hybridization.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 180, doi. 10.1159/000015023
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Assignment[sup 1] of Erbb2 to rat chromosome band 10q32.1 by in situ hybridization.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 182, doi. 10.1159/000015024
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FHIT gene transcript alterations occur frequently in myeloproliferative and myelodysplastic diseases.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 183, doi. 10.1159/000015025
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Assignment[sup 1] of the Smad7 gene (MADH7) to human chromosome 18q21.1 by fluorescence in situ hybridization.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 189, doi. 10.1159/000015026
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Cloning and mapping of SMARCA5 encoding hSNF2H, a novel human homologue of Drosophila ISWI.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 191, doi. 10.1159/000015027
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Cloning and genomic mapping of the mouse matrin 3 gene and its pseudogenes.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 194, doi. 10.1159/000015028
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Identification and in situ hybridization mapping of a mouse Tpd52l1 (D53) orthologue to chromosome 10A4–B2.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 199, doi. 10.1159/000015029
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Comparative FISH-mapping of the prion protein gene (PRNP) on cattle, river buffalo, sheep and goat chromosomes.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 202, doi. 10.1159/000015030
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Physical and linkage mapping of the gene for the α3 chain of type IX collagen, COL9A3, to human chromosome 20q13.3.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 205, doi. 10.1159/000015031
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Comparative FISH mapping of mouse and rat homologues of twenty-five human X-linked genes.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 208, doi. 10.1159/000015032
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Assignment of the mouse and cow CXC chemokine genes.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 213, doi. 10.1159/000015033
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Cytogenetic localization of cancer-related genes in the rat and comparative mapping studies in human and mouse.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 217, doi. 10.1159/000015034
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Cat eye syndrome chromosome breakpoint clustering: identification of two intervals also associated with 22q11 deletion syndrome breakpoints.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 222, doi. 10.1159/000015035
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Physical mapping of the t(12;22) translocation breakpoints in a family with a complex type of 3/3′/4 synpolydactyly.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 229, doi. 10.1159/000015036
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Assignment of the human erythrocyte acylphosphatase gene (ACYP1) to chromosome band 14q24.3.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 235, doi. 10.1159/000015037
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Comparative mapping of two adjacent regions of MMU19 with their human counterpart on HSA11q13.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 237, doi. 10.1159/000015038
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Expressed copies of the MN7 (D15F37) gene family map close to the common deletion breakpoints in the Prader-Willi/Angelman syndromes.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 247, doi. 10.1159/000015039
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Chromosome identification in human oocytes and polar bodies by spectral karyotyping.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 254, doi. 10.1159/000015040
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High-resolution mapping of the X-linked lymphoproliferative syndrome region by FISH on combed DNA.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 259, doi. 10.1159/000015041
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Murine and human TSPYL genes: novel members of the TSPY-SET-NAP1L1 family.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 265, doi. 10.1159/000015042
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The human gene encoding SCYB9B, a putative novel CXC chemokine, maps to human chromosome 4q21 like the closely related genes for MIG (SCYB9) and INP10 (SCYB10).
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 271, doi. 10.1159/000015043
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Assignment[sup 1] of Sp genes to rat chromosome bands 7q36 (Sp1) , 10q31→q32.1 (Sp2) , 3q24→q31 (Sp3) and 6q33 (Sp4) and of the SP2 gene to human chromosome bands 17q21.3→q22 by in situ hybridization.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 273, doi. 10.1159/000015044
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The INSL4 gene maps close to WI-5527 at 9p24.1→p23.3 clustered with two relaxin genes and outside the critical region for the monosomy 9p syndrome.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 275, doi. 10.1159/000015045
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Human serine/threonine protein kinase EMK1: genomic structure and cDNA cloning of isoforms produced by alternative splicing.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 278, doi. 10.1159/000015046
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Assignment[sup 1] of the ZYX gene for the LIM protein zyxin to human chromosome bands 7q34→q35 by in situ hybridization.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 283, doi. 10.1159/000015047
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Assignment[sup 1] of the BMPR1A and BMPR1B genes to human chromosome 10q22.3 and 4q23→q24 byin situ hybridization and radiation hybrid map ping.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 285, doi. 10.1159/000015048
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Gene structure and chromosome location of mouse Cd39 coding for an ecto-apyrase.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 287, doi. 10.1159/000015049
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Assignment[sup 1] of the cyclin-dependent kinase inhibitor genes Cdkn2a and Cdkn2b to rat chromosome bands 5q32→q34 and 5q31→q33, respectively by fluorescence in situ hybridization, using small PCR-generated probes.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 290, doi. 10.1159/000015050
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Assignment[sup 1] of human fatty-acid-Coenzyme A ligase, very long-chain 1 gene (FACVL1) to human chromosome band 15q21.2 by fluorescence in situ hybridization.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 292, doi. 10.1159/000015051
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Assignment[sup 1] of Sox4 to mouse chromosome 13 bands A3–A5 by fluorescence in situ hybridization; refinement[sup 2] of the human SOX4 location to 6p22.3 and of SOX20 to chromosome 17p12.3.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 294, doi. 10.1159/000015052
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Author Index.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 296, doi. 10.1159/000015053
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Subject Index.
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- Cytogenetics & Cell Genetics, 1998, v. 81, n. 3/4, p. 301, doi. 10.1159/000015054
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