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

A retrospective study of 69 patients with t(6;9)(p23;q34) AML emphasizes the need for a prospective, multicenter initiative for rare 'poor prognosis' myeloid malignanciesSLOVAK, M. L; GUNDACKER, H; WILLMAN, C. L et al.Leukemia. 2006, Vol 20, Num 7, pp 1295-1297, issn 0887-6924, 3 p.Article

Duplication of 7p : Further delineation of the phenotype and restriction of the critical region to the distal part of the short armREISH, O; BERRY, S. A; DEWALD, G et al.American journal of medical genetics. 1996, Vol 61, Num 1, pp 21-25, issn 0148-7299Article

Proficiency testing in clinical cytogenetics : a 6-year experience with photographs, fixed cells, and fresh bloodHOELTGE, G. A; DEWALD, G; PALMER, C. G et al.Archives of pathology & laboratory medicine (1976). 1993, Vol 117, Num 8, pp 776-779, issn 0363-0153Article

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

Heterogeneity of cultured leukemic lymphoid progenitor cells from B cell precursor acute lymphoblastic leukemia (ALL) patientsUCKUN, F. M; KERSEY, J. H; LAMPKIN, B et al.The Journal of clinical investigation. 1987, Vol 80, Num 3, pp 639-646, issn 0021-9738Article

A multicenter investigation with D-FISH BCR/ABL1 probesDEWALD, G; STALLARD, R; HOELTGE, G. A et al.Cancer genetics and cytogenetics. 2000, Vol 116, Num 2, pp 97-104, issn 0165-4608Article

The human complement C8G gene, a member of the lipocalin gene family : polymorphisms and mapping to chromosome 9q34.3DEWALD, G; CICHON, S; BRYANT, S. P et al.Annals of human genetics. 1996, Vol 60, pp 281-291, issn 0003-4800, 4Article

A HhaI polymorphism in the human MEP1A gene encoding the alpha subunit of the metalloendopeptidase meprinDEWALD, G; SCHILDHAUS, H.-U; MÜCHER, G et al.Human heredity. 1996, Vol 46, Num 5, pp 298-300, issn 0001-5652Article

Clinical phenotype associated with terminal 2q37 deletionCONRAD, B; DEWALD, G; CHRISTENSEN, E et al.Clinical genetics. 1995, Vol 48, Num 3, pp 134-139, issn 0009-9163Article

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