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Authors: BEIN G DRILLER B SCHURMANN M SCHNEIDER PM KIRCHNER H
Citation: G. Bein et al., PSEUDO-EXCLUSION FROM PATERNITY DUE TO MATERNAL UNIPARENTAL DISOMY-16, International journal of legal medicine, 111(6), 1998, pp. 328-330

Authors: WAIYAWUTH W ZHANG L RITTNER C SCHNEIDER PM
Citation: W. Waiyawuth et al., GENETIC-ANALYSIS OF THE SHORT TANDEM REPEAT SYSTEM D12S391 IN THE GERMAN AND 3 ASIAN POPULATIONS, Forensic science international, 94(1-2), 1998, pp. 25-31

Authors: HOHLER T WUNSCHEL M GERKEN G SCHNEIDER PM ZUMBUSCHENFELDE KHM RITTNER C
Citation: T. Hohler et al., NO ASSOCIATION BETWEEN MANNOSE-BINDING LECTIN ALLELES AND SUSCEPTIBILITY TO CHRONIC HEPATITIS-B VIRUS-INFECTION IN GERMAN PATIENTS, Experimental and clinical immunogenetics, 15(3), 1998, pp. 130-133

Authors: HOHLER T MEYER CU NOTGHI A STRADMANNBELLINGHAUSEN B SCHNEIDER PM STARKE R ZEPP F SANGER R CLEMENS R ZUMBUSCHENFELDE KHM RITTNER C
Citation: T. Hohler et al., THE INFLUENCE OF MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II GENES AND T-CELL V-BETA REPERTOIRE ON RESPONSE TO IMMUNIZATION WITH HBSAG, Human immunology, 59(4), 1998, pp. 212-218

Authors: FREDRIKSON GN GULLSTRAND B SCHNEIDER PM WITZELSCHLOMP K SJOHOLM AG ALPER CA AWDEH Z TRUEDSSON L
Citation: Gn. Fredrikson et al., CHARACTERIZATION OF NONEXPRESSED C4 GENES IN A CASE OF COMPLETE C4 DEFICIENCY - IDENTIFICATION OF A NOVEL POINT MUTATION LEADING TO A PREMATURE STOP CODON, Human immunology, 59(11), 1998, pp. 713-719

Authors: MORLEY BJ BARTOK I SPATH PJ VYSE TJ SCHNEIDER PM WALPORT MJ
Citation: Bj. Morley et al., MOLECULAR-BASIS OF HEREDITARY FACTOR-I DEFICIENCY, Molecular immunology, 35(6-7), 1998, pp. 54-54

Authors: FRANK A STRADMANNBELLINGHAUSEN B SCHNEIDER PM RITTNER C HOHLER T
Citation: A. Frank et al., MOLECULAR-BASIS OF SEVERAL RARE VARIANTS AND GENOMIC ORGANIZATION OF THE HUMAN C3 GENE, Molecular immunology, 35(6-7), 1998, pp. 297-297

Authors: WITZELSCHLOMP K RITTNER C SCHNEIDER PM
Citation: K. Witzelschlomp et al., STRUCTURAL ORGANIZATION, DEFICIENCY MUTATIONS AND GENETIC-POLYMORPHISM OF THE HUMAN-COMPLEMENT C9 GENE, Molecular immunology, 35(6-7), 1998, pp. 298-298

Authors: HOHLER T KRUGER A GERKEN G SCHNEIDER PM ZUMBUSCHENFELDE KHM RITTNER C
Citation: T. Hohler et al., TURNER NECROSIS FACTOR-ALPHA PROMOTER POLYMORPHISM AT POSITION-238 ISASSOCIATED WITH CHRONIC ACTIVE HEPATITIS-C INFECTION, Journal of medical virology, 54(3), 1998, pp. 173-177

Authors: WITZELSCHLOMP K HOBART MJ FERNIE BA ORREN A WURZNER R RITTNER C KAUFMANN T SCHNEIDER PM
Citation: K. Witzelschlomp et al., HETEROGENEITY IN THE GENETIC-BASIS OF HUMAN-COMPLEMENT C9 DEFICIENCY, Immunogenetics (New York), 48(2), 1998, pp. 144-147

Authors: HORIUCHI T NISHIZAKA H KOJIMA T SAWABE T NIHO Y SCHNEIDER PM INABA S SAKAI K HAYASHI K HASHIMURA C FUKUMORI Y
Citation: T. Horiuchi et al., A NONSENSE MUTATION AT ARG(95) IS PREDOMINANT IN COMPLEMENT-9 DEFICIENCY IN JAPANESE, The Journal of immunology, 160(3), 1998, pp. 1509-1513

Authors: HOHLER T KRUGER A GERKEN G SCHNEIDER PM ZUMBUSCHENFELDE KHM RITTNER C
Citation: T. Hohler et al., A TUMOR-NECROSIS-FACTOR-ALPHA (TNF-ALPHA) PROMOTER POLYMORPHISM IS ASSOCIATED WITH CHRONIC HEPATITIS-B INFECTION, Clinical and experimental immunology, 111(3), 1998, pp. 579-582

Authors: HOHLER T SCHAAPER T SCHNEIDER PM ZUMBUUSCHENFELDE KHM MARKERHERMANN E
Citation: T. Hohler et al., DIFFERENCES IN TNF-ALPHA PROMOTER ALLELE FREQUENCIES ARE ASSOCIATED WITH ANKYLOSING-SPONDYLITIS IN HLA-B27 POSITIVE INDIVIDUALS, Arthritis and rheumatism, 41(9), 1998, pp. 1934-1934

Authors: HOHLER T SCHAPER T SCHNEIDER PM ZUMBUSCHENFELDE KHM MARKERHERMANN E
Citation: T. Hohler et al., ASSOCIATION OF DIFFERENT TUMOR-NECROSIS-FACTOR-ALPHA PROMOTER ALLELE FREQUENCIES WITH ANKYLOSING-SPONDYLITIS IN HLA-B27 POSITIVE INDIVIDUALS, Arthritis and rheumatism, 41(8), 1998, pp. 1489-1492

Authors: SCHNEIDER PM FELLBAUM C FINK U BOLLSCHWEILER E PRAUER HW
Citation: Pm. Schneider et al., PROGNOSTIC IMPORTANCE OF HISTOMORPHOLOGIC SUBCLASSIFICATION FOR EPITHELIAL THYMIC TUMORS, Annals of surgical oncology, 4(1), 1997, pp. 46-56

Authors: KAYSER M CAGLIA A CORACH D FRETWELL N GEHRIG C GRAZIOSI G HEIDORN F HERRMANN S HERZOG B HIDDING M HONDA K JOBLING M KRAWCZAK M LEIM K MEUSER S MEYER E OESTERREICH W PANDYA A PARSON W PENACINO G PEREZLEZAUN A PICCININI A PRINZ M SCHMITT C SCHNEIDER PM SZIBOR R TEIFELGREDING J WEICHOLD G DEKNIJFF P ROEWER L
Citation: M. Kayser et al., EVALUATION OF Y-CHROMOSOMAL STRS - A MULTICENTER STUDY, International journal of legal medicine, 110(3), 1997, pp. 125

Authors: DEKNIJFF P KAYSER M CAGLIA A CORACH D FRETWELL N GEHRIG C GRAZIOSI G HEIDORN F HERRMANN S HERZOG B HIDDING M HONDA K JOBLING M KRAWCZAK M LEIM K MEUSER S MEYER E OESTERREICH W PANDYA A PARSON W PENACINO G PEREZLEZAUN A PICCININI A PRINZ M SCHMITT C SCHNEIDER PM SZIBOR R TEIFELGREDING J WEICHHOLD G ROEWER L
Citation: P. Deknijff et al., CHROMOSOME-Y MICROSATELLITES - POPULATION GENETIC AND EVOLUTIONARY ASPECTS, International journal of legal medicine, 110(3), 1997, pp. 134-149

Authors: SCHNEIDER PM RITTER C MARTIN PD
Citation: Pm. Schneider et al., SPECIAL ISSUE - PROCEEDINGS OF THE EUROPEAN SYMPOSIUM - ETHICAL AND LEGAL ISSUES OF DNA TYPING IN FORENSIC MEDICINE, Forensic science international, 88(1), 1997, pp. 1-2

Authors: SCHNEIDER PM
Citation: Pm. Schneider, BASIC ISSUES IN FORENSIC DNA TYPING, Forensic science international, 88(1), 1997, pp. 17-22

Authors: SCHMITTER H SCHNEIDER PM
Citation: H. Schmitter et Pm. Schneider, LEGAL-ASPECTS OF FORENSIC DNA ANALYSIS IN GERMANY, Forensic science international, 88(1), 1997, pp. 95-98

Authors: MORLING N RITTNER C SCHMITTER H BEYLEVELD D MARTIN PD SCHNEIDER PM SCHEITHAUER R WERRETT DJ OLAISEN B KLOOSTERMAN A
Citation: N. Morling et al., SPECIAL ISSUE - PROCEEDINGS OF THE EUROPEAN SYMPOSIUM - ETHICAL AND LEGAL ISSUES OF DNA TYPING IN FORENSIC MEDICINE - SUMMARY OF THE DISCUSSION, Forensic science international, 88(1), 1997, pp. 99-105

Authors: SCHNEIDER PM
Citation: Pm. Schneider, CHANGES IN THE DNA PROFILE CAUSED BY TOXIC-SUBSTANCES, Forensic science international, 86(1-2), 1997, pp. 145-148

Authors: SCHNEIDER PM
Citation: Pm. Schneider, MOLECULAR PATHOGENESIS OF ADENOCARCINOMAS IN BARRETTS-ESOPHAGUS - ROLE OF TUMOR-SUPPRESSOR GENE P53 (VOL 20, PG 36, 1997), Onkologie, 20(2), 1997, pp. 104-104

Authors: SCHNEIDER PM CASSON AG HOLSCHER AH SCHWEIGHART S MIZUMOTO S SIEWERT JR ROTH JA
Citation: Pm. Schneider et al., MOLECULAR PATHOGENESIS OF ADENOCARCINOMAS IN BARRETTS-ESOPHAGUS - ROLE OF THE TUMOR-SUPPRESSOR GENE P53, Onkologie, 20(1), 1997, pp. 36-40

Authors: WEGREMERS S BRENDEN M SCHWARZ E WITZEL K SCHNEIDER PM GUERRA LK REHFELDT IR LIMA MT HARTMANN D PETZLERLER ML DEMESSIAS IJT MAUFF G
Citation: S. Wegremers et al., MAJOR HISTOCOMPATIBILITY COMPLEX (MHC) CLASS-III GENETICS IN 2 AMERINDIAN TRIBES FROM SOUTHERN BRAZIL - THE KAINGANG AND THE GUARANI, Human genetics, 100(5-6), 1997, pp. 548-556
Risultati: 1-25 | 26-50 | 51-71