Works matching IS 0301-0171 AND VI 82 AND IP 1/2 AND DT 1998
Results: 33
Structure and refinement of the physical mapping of the γ-glutamylcysteine ligase regulatory subunit (GLCLR) gene to chromosome 1p22.1 within the critically deleted region of human malignant mesothelioma.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 91, doi. 10.1159/000015072
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Report of the seventh international workshop on human chromosome 21 mapping 1997.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 1, doi. 10.1159/000015055
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The cytogenetic and molecular characterization of benign and malignant soft tissue tumors.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 13, doi. 10.1159/000015056
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Assignment<FOOTREF>[sup 1] </FOOTREF> of protein kinase Cη (Pkch ) to mouse chromosome band 12C3–D2 by in situ hybridization.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 30, doi. 10.1159/000015057
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Assignment<FOOTREF>[sup 1] </FOOTREF> of IκB kinase β (IKBKB) to human chromosome band 8p12→p11 by in situ hybridization.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 32, doi. 10.1159/000015058
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Assignment of the human oxidized low-density lipoprotein receptor gene (OLR1) to chromosome 12p13.1→p12.3, and identification of a polymorphic CA-repeat marker in the OLR1 gene.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 34, doi. 10.1159/000015059
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Genomic organization of the bovine aromatase encoding gene and a homologous pseudogene as revealed by DNA fiber FISH.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 37, doi. 10.1159/000015060
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Cloning of TCFL5 encoding a novel human basic helix-loop-helix motif protein that is specifically expressed in primary spermatocytes at the pachytene stage.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 41, doi. 10.1159/000015061
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Linkage mapping of Lims1l, the murine homolog of the human LIM domain gene PINCH, to mouse Chromosome 10.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 46, doi. 10.1159/000015062
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Hemizygous deletion of the HPC-1/syntaxin 1A gene (STX1A) in patients with Williams syndrome.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 49, doi. 10.1159/000015063
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Pathogenetics of 45,X/46,XY gonadal mosaicism.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 52, doi. 10.1159/000015064
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Position effect of translocations involving the inactive X chromosome: physical linkage to XIC/XIST does not lead to long-range de novo inactivation in human differentiated cells.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 58, doi. 10.1159/000015065
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Genetic mapping of mouse centromere protein (Incenp and Cenpe ) genes.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 67, doi. 10.1159/000015066
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Localization of FCGR1 encoding Fcγ receptor class I in primates: molecular evidence for two pericentric inversions during the evolution of human chromosome 1.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 71, doi. 10.1159/000015067
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Analysis of chromosome aberrations in a mammary carcinoma cell line from a dog by using canine painting probes.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 75, doi. 10.1159/000015068
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A baboon (Papio hamadryas) with an isochromosome for the long arm of the X.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 80, doi. 10.1159/000015069
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Baboon/human homologies examined by spectral karyotyping (SKY): a visual comparison.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 83, doi. 10.1159/000015070
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Structure and chromosome mapping of the human small maf genes MAFG and MAFK.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 88, doi. 10.1159/000015071
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Assignment of CASP8<FOOTREF>[sup 1] </FOOTREF> to human chromosome band 2q33→q34 and Casp8 <FOOTREF>[sup 2] </FOOTREF> to the murine syntenic region on chromosome 1B-proximal C by in situ hybridization.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 95, doi. 10.1159/000015073
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Assignment<FOOTREF>[sup 1] </FOOTREF> of the melanocortin 4 receptor (MC4R) gene to human chromosome band 18q22 by in situ hybridisation and radiation hybrid mapping.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 97, doi. 10.1159/000015074
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Assignment<FOOTREF>[sup 1] </FOOTREF> of the E1A-regulated transcription factor E4F gene (E4F1) to human chromosome band 16p13.3 by in situ hybridization and somatic cell hybrids.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 99, doi. 10.1159/000015075
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Genomic structure of a novel human gene (XYLB) on chromosome 3p22→p21.3 encoding a xylulokinase-like protein.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 101, doi. 10.1159/000015076
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Assignment of the IκB-β gene NFKBIB to human chromosome band 19q13.1 by in situ hybridization.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 105, doi. 10.1159/000015077
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Fine mapping of 12 previously unassigned EST clones to individual YACs in the familial Alzheimer’s disease (FAD) region of chromosome 14q24.3.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 107, doi. 10.1159/000015078
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Assignment<FOOTREF>[sup 1] </FOOTREF> of the horse progesterone receptor (PGR) and estrogen receptor (ESR1) genes to horse chromosomes 7 and 31, respectively, by in situ hybridization.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 110, doi. 10.1159/000015079
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Assignment<FOOTREF>[sup 1] </FOOTREF> of the horse mitochondrial glutamate oxaloacetate transaminase 2 (GOT2) and v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog (KIT) to horse chromosome 3 by in situ hybridization.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 112, doi. 10.1159/000015080
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Mapping<FOOTREF>[sup 1] </FOOTREF> of the NDUFA2, NDUFA6, NDUFA7, NDUFB8, and NDUFS8 electron transport chain genes by intron based radiation hybrid mapping.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 114, doi. 10.1159/000015081
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lntron based radiation hybrid mapping of 15 complex I genes of the human electron transport chain.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 115, doi. 10.1159/000015082
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Assignment<FOOTREF>[sup 1] </FOOTREF> of candidate DNA methyltransferase gene (DNMT2) to human chromosome band 10p15.1 by in situ hybridization.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 120, doi. 10.1159/000015083
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Assignment<FOOTREF>[sup 1] </FOOTREF> of FRA1H common fragile site to human chromosome band 1q42.1 proximal to the nuclear NAD[sup +] ADP-ribosyltransferase gene (ADPRT) and to the main 5S rRNA gene locus.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 121, doi. 10.1159/000015084
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Chromosomal localization<FOOTREF>[sup 1] </FOOTREF> of the human cytoplasmic dynein heavy chain gene DNCH2 to 11q21→q22.1.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 123, doi. 10.1159/000015085
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Autosomal-dominant, prelingual, nonprogressive sensorineural hearing loss: localization of the gene (DFNA8) to chromosome 11q by linkage in an Austrian family.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 126, doi. 10.1159/000015086
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Abstracts of the 35th American Cytogenetics Conference.
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- Cytogenetics & Cell Genetics, 1998, v. 82, n. 1/2, p. 131, doi. 10.1159/000015087
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- Article