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Results: 19
Authors:
MUHLMANN J
THALER J
HILBE W
BECHTER O
ERDEL M
UTERMANN G
DUBA HC
Citation: J. Muhlmann et al., FLUORESCENCE IN-SITU HYBRIDIZATION (FISH) ON PERIPHERAL-BLOOD SMEARS FOR MONITORING PHILADELPHIA-CHROMOSOME-POSITIVE CHRONIC MYELOID-LEUKEMIA (CML) DURING INTERFERON TREATMENT - A NEW STRATEGY FOR REMISSION ASSESSMENT, Genes, chromosomes & cancer, 21(2), 1998, pp. 90-100
Authors:
VERDORFER I
CULIG Z
HOBISCH A
BARTSCH G
HITTMAIR A
DUBA HC
ERDEL M
Citation: I. Verdorfer et al., CHARACTERIZATION OF A COLLECTING DUCT CARCINOMA BY CYTOGENETIC ANALYSIS AND COMPARATIVE GENOMIC HYBRIDIZATION, International journal of oncology, 13(3), 1998, pp. 461-464
Authors:
DUBA HC
ERDEL M
LOFFLER J
WIRTH J
UTERMANN B
UTERMANN G
Citation: Hc. Duba et al., NAIL-PATELLA SYNDROME IN A CYTOGENETICALLY BALANCED T(9-17)(Q34.1-Q25) CARRIER, European journal of human genetics, 6(1), 1998, pp. 75-79
Authors:
WALDEGGER S
ERDEL M
NAGL UO
BARTH P
RABER G
STEUER S
UTERMANN G
PAULMICHL M
LANG F
Citation: S. Waldegger et al., GENOMIC ORGANIZATION AND CHROMOSOMAL LOCALIZATION OF THE HUMAN SGK PROTEIN-KINASE GENE, Genomics (San Diego, Calif.), 51(2), 1998, pp. 299-302
Authors:
NAGL UO
ERDEL M
BERGMANN F
OEHL B
SCANDELLA E
MUSANTE L
GALIETTA LJV
GSCHWENTNER M
FURST J
SCHMARDA A
HOFER S
UTERMANN G
DEETJEN P
PAULMICHL M
Citation: Uo. Nagl et al., CHARACTERIZATION OF THE HUMAN GENE CODING FOR THE SWELLING-DEPENDENT CHLORIDE CHANNEL I-CLN AT POSITION 11Q13.5-14.1 (CLNS1A) AND FURTHER CHARACTERIZATION OF THE CHROMOSOME-6 (CLNS1B) LOCALIZATION, Gene, 209(1-2), 1998, pp. 59-63
Authors:
ERDEL M
LAICH A
UTERMANN G
WERNER ER
WERNERFELMAYER G
Citation: M. Erdel et al., 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), Cytogenetics and cell genetics, 81(3-4), 1998, pp. 271-272
Authors:
SCHERER G
HELD M
ERDEL M
MESCHEDE D
HORST J
LESNIEWICZ R
MIDRO AT
Citation: G. Scherer et al., 3 NOVEL SRY MUTATIONS IN XY GONADAL-DYSGENESIS AND THE ENIGMA OF XY GONADAL-DYSGENESIS CASES WITHOUT SRY MUTATIONS, Cytogenetics and cell genetics, 80(1-4), 1998, pp. 188-192
Authors:
FITZKY BU
WITSCHBAUMGARTNER M
ERDEL M
GLOSSMANN H
UTERMANN G
MOEBIUS FF
Citation: Bu. Fitzky et al., MUTATIONS IN THE DELTA-7-STEROL REDUCTASE GENE IN PATIENTS WITH THE SMITH-LEMLI-OPITZ-SYNDROME, Naunyn-Schmiedeberg's archives of pharmacology, 357(4), 1998, pp. 22-22
Authors:
FITZKY BU
WITSCHBAUMGARTNER M
ERDEL M
LEE JN
PAIK YK
GLOSSMANN H
UTERMANN G
MOEBIUS FF
Citation: Bu. Fitzky et al., MUTATIONS IN THE DELTA-7-STEROL REDUCTASE GENE IN PATIENTS WITH THE SMITH-LEMLI-OPITZ-SYNDROME, Proceedings of the National Academy of Sciences of the United Statesof America, 95(14), 1998, pp. 8181-8186
Authors:
KOFLER K
KOCHL S
PARSON W
ERDEL M
UTERMANN G
BAIER G
Citation: K. Kofler et al., MOLECULAR CHARACTERIZATION OF THE HUMAN PROTEIN-KINASE-C 0-ASTERISK GENE LOCUS (PRKCQ), MGG. Molecular & general genetics, 259(4), 1998, pp. 398-403
Authors:
EIBL B
EBNER S
DUBA C
BOCK G
ROMANI N
ERDEL M
GACHTER A
NIEDERWIESER D
SCHULER G
Citation: B. Eibl et al., DENDRITIC CELLS GENERATED FROM BLOOD PRECURSORS OF CHRONIC MYELOGENOUS LEUKEMIA PATIENTS CARRY THE PHILADELPHIA TRANSLOCATION AND CAN INDUCE A CML-SPECIFIC PRIMARY CYTOTOXIC T-CELL RESPONSE, Genes, chromosomes & cancer, 20(3), 1997, pp. 215-223
CHARACTERIZATION OF AN INTRONLESS HUMAN GENE LOCUS FOR THE SWELLING DEPENDENT ANION CHANNEL (CLNSIB)
Authors:
SCANDELLA E
NAGL UO
ERDEL M
BERGMANN F
OEHL B
MUSANTE L
GSCHWENTNER M
FURST J
SCHMARDA A
DEETJEN P
PAULMICHL M
Citation: E. Scandella et al., CHARACTERIZATION OF AN INTRONLESS HUMAN GENE LOCUS FOR THE SWELLING DEPENDENT ANION CHANNEL (CLNSIB), The FASEB journal, 11(9), 1997, pp. 538-538
Authors:
NAGL UO
ERDEL M
SCANDELLA E
OEHL B
BERGMANN F
MUSANTE L
GSCHWENTNER M
FURST J
SCHMARDA A
DEETJEN P
PAULMICHL M
Citation: Uo. Nagl et al., CHARACTERIZATION OF THE HUMAN GENE CODING FOR THE SWELLING-DEPENDENT ANION CHANNEL 1C1N (CLNSLA), The FASEB journal, 11(9), 1997, pp. 539-539
Authors:
WEISKIRCHEN R
ERDEL M
UTERMANN G
BISTER K
Citation: R. Weiskirchen et al., CLONING, STRUCTURAL-ANALYSIS, AND CHROMOSOMAL LOCALIZATION OF THE HUMAN CSRP2 GENE ENCODING THE LIM DOMAIN PROTEIN CRP2, Genomics, 44(1), 1997, pp. 83-93
Authors:
ERDEL M
DUBA HC
VERDORFER I
LINGENHEL A
GEIGER R
GUTENBERGER KH
LUDESCHER E
UTERMANN B
UTERMANN G
Citation: M. Erdel et al., COMPARATIVE GENOMIC HYBRIDIZATION REVEALS A PARTIAL DE-NOVO TRISOMY 6Q23-QTER IN AN INFANT WITH CONGENITAL-MALFORMATIONS - DELINEATION OF THE PHENOTYPE, Human genetics, 99(5), 1997, pp. 596-601
Authors:
DUBA HC
ERDEL M
LOFFLER J
BEREUTHER L
FISCHER H
UTERMANN B
UTERMANN G
Citation: Hc. Duba et al., DETECTION OF A DE-NOVO DUPLICATION OF 1Q32-QTER BY FLUORESCENCE IN-SITU HYBRIDIZATION IN A BOY WITH MULTIPLE MALFORMATIONS - FURTHER DELINEATION OF THE TRISOMY 1Q SYNDROME, Journal of Medical Genetics, 34(4), 1997, pp. 309-313
Authors:
NAGL UO
ERDEL M
SCHMARDA A
SERI M
PINGGERA GM
GSCHWENTNER M
DUBA C
GALIETTA LJV
DEETJEN P
UTERMANN G
PAULMICHL M
Citation: Uo. Nagl et al., CHROMOSOMAL LOCALIZATION OF THE GENES (CLNS1A AND CLNS1B) CODING FOR THE SWELLING-DEPENDENT CHLORIDE CHANNEL I-CLN, Genomics, 38(3), 1996, pp. 438-441
Authors:
ERDEL M
SCHUFFENHAUER S
BUCHHOLZ B
BARTHWITTE U
KOCHL S
UTERMANN B
DUBA HC
UTERMANN G
Citation: M. Erdel et al., ROUTINE SCREENING FOR MICRODELETIONS BY FISH IN 77 PATIENTS SUSPECTEDOF HAVING PRADER-WILLI OR ANGELMAN SYNDROMES USING YAC CLONE 273A2 (D15S10), Human genetics, 97(6), 1996, pp. 784-793
Authors:
ERDEL M
BAIERBITTERLICH G
DUBA C
ISAKOV N
ALTMAN A
UTERMANN G
BAIER G
Citation: M. Erdel et al., MAPPING OF THE HUMAN PROTEIN-KINASE C-THETA (PRKCQ) GENE LOCUS TO THESHORT ARM OF CHROMOSOME-10 (10P15) BY FISH, Genomics, 25(2), 1995, pp. 595-597
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