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:
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
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
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:
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
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