Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("RINGELHANN B")

Results 1 to 7 of 7

  • Page / 1
Export

Selection :

  • and

ANOMALY IN THE GAMMA CHAIN HETEROGENEITY OF THE NEWBORN.HUISMAN THJ; SCHROEDER WA; FELICE A et al.1977; NATURE; G.B.; DA. 1977; VOL. 265; NO 5589; PP. 63-65; BIBL. 13 REF.Article

A NEW LOOK AT THE PROTECTION OF HEMOGLOBIN AS AND AC GENOTYPES AGAINST PLASMODIUM FALCIPARUM INFECTION: A CENSUS TRACT APPROACHRINGELHANN B; HATHORN MKS; JILLY P et al.1976; AMER. J. HUM. GENET.; U.S.A.; DA. 1976; VOL. 28; NO 3; PP. 270-279; BIBL. 1 P. 1/2Article

HEMOGLOBINOPATHIES IN HUNGARYSZELENYI J; HORANYI M; FOLDI J et al.1983; HEMOGLOBIN; ISSN 0363-0269; USA; DA. 1983; VOL. 7; NO 3; PP. 297-299; BIBL. 13 REF.Article

HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN, BETA THALASSEMIA, AND THE HEMOGLOBIN DELTA -BETA LOCUS: FURTHER FAMILY DATA AND GENETIC INTERPRETATIONSBETHLENFALYAY NC; MOTULSKY AG; RINGELHANN B et al.1975; AMER. J. HUM. GENET.; U.S.A.; DA. 1975; VOL. 27; NO 2; PP. 140-154; BIBL. 2 P.Article

HEMOGLOBIN ALPHA CHAIN DEFICIENCY IN BLACK CHILDREN WITH VARIABLE QUANTITIES OF HEMOGLOBIN BART'S AT BIRTH.ALTAY C; RINGELHANN B; YAWSON GI et al.1977; PEDIATR. RES.; U.S.A.; DA. 1977; VOL. 11; NO 2; PP. 147-152; BIBL. 34 REF.Article

HOMOZYGOTES FOR THE HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN: THE RATIO OF GY CHAINS AND BIOSYNTHETIC STUDIES.RINGELHANN B; ACQUAYE CTA; OLDHAM JH et al.1977; BIOCHEM. GENET.; U.S.A.; DA. 1977; VOL. 15; NO 11-12; PP. 1083-1096; BIBL. 1 P. 1/2Article

Molecular characterization of β-thalassemia in HungaryRINGELHANN, B; SZELENYI, J. G; HORANYI, M et al.Human genetics. 1993, Vol 92, Num 4, pp 385-387, issn 0340-6717Article

  • Page / 1