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AUTOMATED VIDEODENSITOMETRY OF HUMAN CHROMOSOMES.GORDON H; DEWALD G.1974; BIRTH DEFECTS ORIGIN ARTICLE SER.; U.S.A.; DA. 1974; VOL. 10; NO 8; PP. 87-91Article

Polymorphism of the seventh component of complement (C7) in a healthy Caucasian population: an immunoblotting study with neuraminidase-treated samplesDEWALD, G.Annales de l'Institut Pasteur. Immunologie. 1988, Vol 139, Num 5, pp 507-515, issn 0769-2625Article

POLYMORPHISM OF THE SECOND COMPONENT OF HUMAN COMPLEMENT (C2): OBSERVATION OF THE RARE PHENOTYPE C22(=C2B) AND DATA ON THE LOCALIZATION OF THE C2 LOCUS IN THE HLA REGIONDEWALD G; RITTNER C.1979; VOX SANG.; CHE; DA. 1979; VOL. 37; NO 1; PP. 47-54; BIBL. 27 REF.Article

USEFULNESS OF CHROMOSOME EXAMINATION IN THE DIAGNOSIS OF MALIGNANT PLEURAL EFFUSIONS.DEWALD G; DINES DE; WEILAND LH et al.1976; NEW ENGL. J. MED.; U.S.A.; DA. 1976; VOL. 295; NO 27; PP. 1494-1500; BIBL. 23 REF.Article

SISTER CHROMATID EXCHANGES IN BLOOM'S SYNDROME.DICKEN CH; DEWALD G; GORDON H et al.1978; ARCH. DERMATOL.; U.S.A.; DA. 1978; VOL. 114; NO 5; PP. 755-760; BIBL. 17 REF.Article

A common amino acid polymorphism in complement component C1RNÖTHEN, M. M; DEWALD, G.Human molecular genetics (Print). 1994, Vol 3, Num 1, issn 0964-6906, p. 217Article

Polyarenemethines containing alternating phenyl/dihydroanthracene unitsHANACK, M; DEWALD, G.Synthetic metals. 1989, Vol 33, Num 3, pp 409-414, issn 0379-6779Article

C6-POLYMORPHISMUS DER SECHSTEN KOMPLEMENTKOMPONENTE: EIN NEUES, AUSSAGEKRAEFIGES SYSTEM IN DER ABSTAMMUNGSBEGUTACHTUNG = POLYMORPHISME C6 DE LA SIXIEME COMPOSANTE DU COMPLEMENT: UN NOUVEAU SYSTEME VALABLE DANS LES EXPERTISES DE PATERNITERITTNER C; DEWALD G; BERGHOFF E et al.1979; Z. RECHTSMED.; DEU; DA. 1979; VOL. 83; NO 1; PP. 17-25; ABS. ENG; BIBL. 11 REF.Article

FAILURE OF INACTIVATION OF DUCHENNE DYSTROPHY X-CHROMOSOME IN ONE OF FEMALE IDENTICAL TWINS.GOMEZ MR; ENGEL AG; DEWALD G et al.1977; NEUROLOGY; U.S.A.; DA. 1977; VOL. 27; NO 6; PP. 537-541; BIBL. 18 REF.Article

154 Chromosome anomalies in hematologic malignanciesDEWALD, G. W; STUPCA, P.Leukemia research. 2000, Vol 24, Num 6, pp 487-489, issn 0145-2126Article

Dinucleotide repeat polymorphism at the human CD59 locusNÖTHEN, M. M; DEWALD, G.Clinical genetics. 1995, Vol 47, Num 3, pp 165-166, issn 0009-9163Article

Identification of a small supernumerary ring chromosome 8 by fluorescent in situ hybridization in a child with developmental delay and minor anomaliesMELNYK, A. R; DEWALD, G.American journal of medical genetics. 1994, Vol 50, Num 1, pp 12-14, issn 0148-7299Article

ORIGIN OF CHI 46, XX/46, XY CHIMERISM IN A HUMAN TRUE HERMAPHRODITEDEWALD G; HAYMOND MW; SPURBECK JL et al.1980; SCIENCE; USA; DA. 1980; VOL. 207; NO 4428; PP. 321-323; BIBL. 16 REF.Article

EXCLUSION OF HLA LOCUS FROM A LARGE PORTION OF THE LONG ARM OF CHROMOSOME 6.KUEPPERS F; DEWALD G; GORDON H et al.1977; HUM. HERED.; SWITZ.; DA. 1977; VOL. 27; NO 4; PP. 242-246; BIBL. 9 REF.Article

A DIPLOID-TRIPHOID HUMAN MOSAIC WITH CYTOGENETIC EVIDENCE OF DOUBLE FERTILIZATION.DEWALD G; ALVAREZ MN; CLOUTIER MD et al.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 8; NO 2; PP. 149-160; BIBL. 1 P.Article

FEMALE PHENOTYPE AND MULTIPLE ABNORMALITIES IN SIBS WITH A Y CHROMOSOME AND PARTIAL X CHROMOSOME DUPLICATION: H-Y ANTIGEN AND XG BLOOD GROUP FINDINGSBERNSTEIN R; JENKINS T; DAWSON B et al.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 4; PP. 291-300; BIBL. 38 REF.Article

Hereditary angio-oedema with normal C1 inhibitor in a family with affected women and menBORK, K; GÜL, D; DEWALD, G et al.British journal of dermatology (1951). 2006, Vol 154, Num 3, pp 542-545, issn 0007-0963, 4 p.Article

Human complement component C8 : molecular basis of the β-chain polymorphismDEWALD, G; HEMMER, S; NÖTHEN, M. M et al.FEBS letters. 1994, Vol 340, Num 3, pp 211-215, issn 0014-5793Article

Polyarenemethylidenes, a new class of low gap polymersHANACK, M; HIEBER, G; DEWALD, G et al.Synthetic metals. 1991, Vol 41, Num 1-2, pp 507-511, issn 0379-6779, 5 p.Conference Paper

Hereditary neuropathy with liability to pressure palsies and inherited brachial plexus neuropathy : two genetically distinct disordersWINDEBANK, A. J; SCHENONE, A; DEWALD, G. W et al.Mayo Clinic proceedings. 1995, Vol 70, Num 8, pp 743-746, issn 0025-6196Article

Polymorphism of human complement component C6 : an amino acid substitution (Glu/Ala) within the second thrombospondin repeat differentiates between the two common allotypes C6 A and C6 BDEWALD, G; NÖTHEN, M. M; CICHON, S et al.Biochemical and biophysical research communications (Print). 1993, Vol 194, Num 1, pp 458-464, issn 0006-291XArticle

Family study on the polymorphism of the sixth and seventh components (C6 and C7) of human complement: linkage and haplotype analysesTOKUNAGA, K; DEWALD, G; OMOTO, K et al.American journal of human genetics. 1986, Vol 39, Num 3, pp 414-419, issn 0002-9297Article

Effect of recombinant gamma interferon on chronic myelogenous leukemia bone marrow progenitorsMCGLAVE, P; MAMUS, S; VILEN, B et al.Experimental hematology. 1987, Vol 15, Num 4, pp 331-335, issn 0301-472XArticle

Pseudomosaicism, true mosaicism, and maternal cell contamination in amniotic fluid processed with in situ culture and robotic harvestingMOERTEL, C. A; STUPCA, P. J; DEWALD, G. W et al.Prenatal diagnosis. 1992, Vol 12, Num 8, pp 671-683, issn 0197-3851Article

Proficiency testing in clinical cytogenetics. The 196 experience of the college of american pathologistsHOELTGE, G. A; DEWALD, G; MILES, J et al.Archives of pathology & laboratory medicine (1976). 1988, Vol 112, Num 11, pp 1085-1190, issn 0363-0153Article

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