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

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

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

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

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

HLA-linked complement polymorphisms (C2, BF) in psoriasisDEWALD, G; LANGE, C.-E; SCHMEEL, E et al.Archives of dermatological research (Print). 1983, Vol 275, Num 5, pp 301-304, issn 0340-3696Article

Subspecialty clinics : HematologyTEFFERI, A; LITZOW, M. R; NOEL, P et al.Mayo Clinic proceedings. 1997, Vol 72, Num 5, pp 445-452, issn 0025-6196Article

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

Possible cytogenetic distinction between lymphoid and myeloid blast crisis in chronic granulocytic leukemiaDIEZ-MARTIN, J. L; DEWALD, G. W; PIERRE, R. V et al.American journal of hematology. 1988, Vol 27, Num 3, pp 194-203, issn 0361-8609Article

Ph¹-negative chronic granulocytic leukemia: a nonentityTRAVIS, L. B; PIERRE, R. V; DEWALD, G. W et al.American journal of clinical pathology. 1986, Vol 85, Num 2, pp 186-193, issn 0002-9173Article

Cytogenetic studies in 174 consecutives patients with preleukemic or myelodysplastic syndromesKNAPP, R. H; DEWALD, G. W; PIERRE, R. V et al.Mayo Clinic proceedings. 1985, Vol 60, Num 8, pp 507-516, issn 0025-6196Article

Establishment of an immature mast cell line from a patient with mast cell leukemiaBUTTERERFIELD, J. H; WEILER, D; DEWALD, G et al.Leukemia research. 1988, Vol 12, Num 4, pp 345-355, issn 0145-2126Article

Detection of hyperdiploid malignant cells in pleural effusions with chromosome-specific probes and fluorescence in situ hybridizationJOHNSON, T. M; KUFFEL, D. G; DEWALD, G. W et al.Mayo Clinic proceedings. 1996, Vol 71, Num 7, pp 643-648, issn 0025-6196Article