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au.\*:("WEHNERT M")

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VITAMIN B12-ABHAENGIGE METHIONINBIOSYNTHESE BEI PSEUDOMONAS AERUGINOSA = BIOSYNTHESE DE METHIONINE DEPENDANTE DE LA VITAMINE B12 CHEZ P.A.WEHNERT M; GUENTHER E; HERRMANN H et al.1975; Z. ALLG. MIKROBIOL.; DTSCH.; DA. 1975; VOL. 15; NO 4; PP. 281-286; ABS. ANGL.; BIBL. 14REF.Article

Characterization of three new deletions at the 5' end of the HPRT structural geneWEHNERT, M; HERRMANN, F. H.Journal of inherited metabolic disease. 1990, Vol 13, Num 2, pp 178-183, issn 0141-8955, 6 p.Article

UNTERSUCHUNGEN ZUR DNS SYNTHESE IN HAUTFIBROBLASTEN VON PSORIATIKERN = ETUDES DE LA SYNTHESE D'ADN DANS LES FIBROBLASTES CUTANES DES MALADES AVEC PSORIASISMACHILL G; CHRISTOFI C; WEHNERT M et al.1978; DERMATOL. MONATSSCHR.; DDR; DA. 1978; VOL. 164; NO 10; PP. 703-710; ABS. ENG; BIBL. 25 REF.Article

ALPHA -L-IDURONIDASE-AKTIVITAET IN FIBROBLASTEN VON PATIENTEN MIT HURLER-SYNDROM. = L'ACTIVITE DE LA ALPHA -U6-IDURONIDASE DANS LES FIBROBLASTES DE MALADES AYANT UN SYNDROME DE HURLERSTAREPRAWO G; GRIMM U; MACHILL G et al.1975; ACTA BIOL. MED. GERM.; ALLEM.; DA. 1975; VOL. 34; NO 6; PP. 1079-1082; BIBL. 9 REF.Article

UNTERSUCHUNGEN ZUR DIFFERENTIALDIAGNOSTIK DER GM2-GANGLIOSIDOSEN = RECHERCHES POUR LE DIAGNOSTIC DIFFERENTIEL DE LA GANGLIOSIDOSE GM2ZSCHIESCHE M; GRIMM U; MACHILL G et al.1979; DTSCHE GESUNDH.-WES.; DDR; DA. 1979; VOL. 34; NO 1; PP. 36-39; ABS. RUS/ENG; BIBL. 28 REF.Article

ZUR PRAENATALEN BIOCHEMISCHEN DIAGNOSE GENETISCH BEDINGTER STOFFWECHSELSTOERUNGEN. = DIAGNOSTIC BIOCHIMIQUE PRENATAL DES TROUBLES METABOLIQUES D'ORIGINE GENETIQUEMACHILL G; KNAPP A; GRIMM U et al.1977; DTSCHE GESUNDH.-WES.; DTSCH.; DA. 1977; VOL. 32; NO 38; PP. 1786-1790; ABS. RUSSE ANGL.; BIBL. 29 REF.Article

Eighteen novel mutations in patients with Lesch-Nyhan syndrome or partial hypoxanthine phosphoribosyltransferase deficiencyWILLERS, I; BOLZ, H; WEHNERT, M et al.Journal of inherited metabolic disease. 1999, Vol 22, Num 7, pp 845-846, issn 0141-8955Article

Two new markers at DXS115 useful for genomic diagnosis in hemophilia AWEHNERT, M; SCHRÖDER, W; HERRMANN, H et al.Thrombotic and haemorrhagic disorders. 1991, Vol 3, Num 1, pp 21-24Article

RFLP analysis for diagnosis of haemophilia A in German Democratic RepublicHERRMANN, F. H; WEHNERT, M; WULFF, K et al.Clinical genetics. 1990, Vol 37, Num 1, pp 12-17, issn 0009-9163Article

A new marker at DXS 115 useful for carrier detection in hemophilia AWEHNERT, M; SCHRÖDER, W; HERRMANN, F. H et al.Human genetics. 1990, Vol 86, Num 1, pp 59-60, issn 0340-6717Article

Partial deletions of factor VIII gene as molecular diagnostic markers in haemophilia AWEHNERT, M; HERRMANN, F. H; WULFF, K et al.Disease markers. 1989, Vol 7, Num 2, pp 113-117, issn 0278-0240Article

Four STR polymorphisms map to a 500 kb region between DXS15 and DXS134WEHNERT, M; REINER, O; CASKEY, C. T et al.Human molecular genetics (Print). 1993, Vol 2, Num 9, issn 0964-6906, p. 1503Article

Molecular heterogeneity of mutations in X-linked diseases (Duchenne muscular dystrophy, hemophilia A, Lesch-Nyhan syndrome, and X-linked ichthyosis)- Results of deletion screeningWEHNERT, M; WULFF, K; HERRMAN, F. H et al.Biologisches Zentralblatt. 1990, Vol 109, Num 2, pp 119-129, issn 0006-3304Article

Genomic organization of the human complex I 13-kDa subunit gene NDUFA5TENSING, K; PATA, I; WITTIG, I et al.Cytogenetics and cell genetics. 1999, Vol 84, Num 1-2, pp 125-127, issn 0301-0171Article

Identification, mapping, and genomic structure of a novel X-chromosomal human gene (SMPX) encoding a small muscular proteinPATZAK, D; ZHUCHENKO, O; LEE, C.-C et al.Human genetics. 1999, Vol 105, Num 5, pp 506-512, issn 0340-6717Article

Structural gene aberrations in mucopolysaccharidosis II (Hunter)WEHNERT, M; HOPWOOD, J. J; SCHRÖDER, W et al.Human genetics. 1992, Vol 89, Num 4, pp 430-432, issn 0340-6717Article

Reliability of the Tønnesen technique for the identification of Hunter carriersPETRUSCHKA, L; MACHILL, G; WEHNERT, M et al.Human genetics. 1983, Vol 64, Num 4, pp 404-406, issn 0340-6717Article

Effects of 30 days of creatine ingestion in older menRAWSON, E. S; WEHNERT, M. L; CLARKSON, P. M et al.European journal of applied physiology and occupational physiology. 1999, Vol 80, Num 2, pp 139-144, issn 0301-5548Article

Deletion screening in patients with Duchenne muscular dystrophyWULFF, K; HERRMANN, F. H; WAPENAAR, M. C et al.Journal of neurology. 1989, Vol 236, Num 8, pp 470-473, issn 0340-5354, 4 p.Article

Expression pattern and further characterization of human MAGED2 and identification of rodent orthologuesLANGNAESE, K; KLOOS, D. U; WEHNERT, M et al.Cytogenetics and cell genetics. 2001, Vol 94, Num 3-4, pp 233-240, issn 0301-0171Article

Isolation, mapping, and genomic structure of an X-linked gene for a subunit of human mitochondrial complex IZHUCHENKO, O; WEHNERT, M; BAILEY, J et al.Genomics (San Diego, Calif.). 1996, Vol 37, Num 3, pp 281-288, issn 0888-7543Article

Further evidence supporting linkage of hereditary neuralgic amyotrophy to chromosome 17qWEHNERT, M; TIMMERMAN, V; SPOELDERS, P et al.Neurology. 1997, Vol 48, Num 6, pp 1719-1721, issn 0028-3878Article

Prenatal diagnosis of phenylketonuria by haplotype analysisWULFF, K; WEHNERT, M; SCHUTZ, M et al.Prenatal diagnosis. 1989, Vol 9, Num 6, pp 421-425, issn 0197-3851Article

Haplotype analysis of classical and mild phenotype of phenylketonuria in the German Democratic RepublicHERRMANN, F. H; WULFF, K; WEHNERT, M et al.Clinical genetics. 1988, Vol 34, Num 3, pp 176-180, issn 0009-9163Article

Large-scale screening for factor V Leiden mutation in a north-eastern German populationSCHRÖDER, W; KOESLING, M; WULFF, K et al.Haemostasis. 1996, Vol 26, Num 5, pp 233-236, issn 0301-0147Article

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