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A PHENOTYPIC ASSOCIATION BETWEEN THE BLOOD GROUP ANTIGEN NEA AND THE RH ANTIGEN DSISTONEN P.1981; MED. BIOL.; ISSN 0302-2137; FIN; DA. 1981; VOL. 59; NO 4; PP. 230-233; BIBL. 9 REF.Article

A "NEW" ALLELE GIVING FURTHER INSIGHT INTO THE LW BLOOD GROUP SYSTEMSISTONEN P; TIPPETT P.1982; VOX SANG.; ISSN 0042-9007; CHE; DA. 1982; VOL. 42; NO 5; PP. 252-255; BIBL. 17 REF.Article

Linkage of the LW blood group locus with the complement C3 and Lutheran blood group lociSISTONEN, P.Annals of human genetics. 1984, Vol 48, Num 3, pp 239-242, issn 0003-4800Article

ON THE HERITABILITY OF SERUM HIGH DENSITY LIPOPROTEIN IN TWINSSISTONEN P; EHNHOLM C.1980; AMER. J. HUM. GENET.; USA; DA. 1980; VOL. 32; NO 1; PP. 1-7; BIBL. 19 REF.Article

GENETICS OF AUTOANTIBODIES IN RELATION TO DISEASE: AN EPIDEMIOLOGICAL STUDY OF TWO POPULATION SERIESAHO K; SISTONEN P; TAKALA J et al.1982; ACTA MED. SCAND.; ISSN 0001-6101; SWE; DA. 1982; VOL. 211; NO 3; PP. 213-218; BIBL. 31 REF.Article

DIAGNOSIS OF TWIN ZYGOSITY BY MAILED QUESTIONNAIRE.SARNA S; KAPRIO J; SISTONEN P et al.1978; HUM. HERED.; SWITZ.; DA. 1978; VOL. 28; NO 4; PP. 241-254; BIBL. 20 REF.Article

SERUM IGE LEVELS IN TWINSSISTONEN P; JOHNSSON V; KOSKENVUO M et al.1980; HUM. HERED.; CHE; DA. 1980; VOL. 30; NO 3; PP. 155-158; BIBL. 6 REF.Article

Haplotype analysis in prenatal diagnosis and carrier identification of Salla diseaseSCHLEUTKER, J; SISTONEN, P; AULA, P et al.Journal of medical genetics. 1996, Vol 33, Num 1, pp 36-41, issn 0022-2593Article

Screening reduces colorectal cancer rate in families with hereditary nonpolypolysis colorectal cancerJÄRVINEN, H. J; MECKLIN, J.-P; SISTONEN, P et al.Gastroenterology (New York, NY. 1943). 1995, Vol 108, Num 5, pp 1405-1411, issn 0016-5085Article

Evidence for a new Rh gene complex producing the rare CX (Rh9) antigen in the Somali population of East AfricaSISTONEN, P; ADEN ABDULLE, O; SAHID, M et al.Transfusion (Philadelphia, PA). 1987, Vol 27, Num 1, pp 66-68, issn 0041-1132Article

The gene for congenital chloride diarrhea maps close to but is distinct from the gene for cystic fibrosis transmembrane conductance regulatorKERE, J; SISTONEN, P; HOLMBERG, C et al.Proceedings of the National Academy of Sciences of the United States of America. 1993, Vol 90, Num 22, pp 10686-10689, issn 0027-8424Article

Linked polymorphic DNA markers in the prediction of X-linked muscular dystrophyLINDLOF, M; SISTONEN, P; DE LA CHAPELLE, A et al.Annals of human genetics. 1987, Vol 51, Num 4, pp 317-328, issn 0003-4800Article

A population genetic study in Finland : comparison of the Finnish- and Swedish-speaking populationsVIRTARANTA-KNOWLES, K; SISTONEN, P; NEVANLINNA, H. R et al.Human heredity. 1991, Vol 41, Num 4, pp 248-264, issn 0001-5652Article

Identical twins with the Rhnull phenotype of the regulator type in a finnish lapp familySISTONEN, P; PALOSUO, T; SNELLMAN, A et al.Vox sanguinis (Basel. 1956). 1985, Vol 48, Num 3, pp 174-177, issn 0042-9007Article

Diastrophic dysplasia gene maps to the distal long arm of chromosome 5HAÊSBACKA, J; KAITILA, I; SISTONEN, P et al.Proceedings of the National Academy of Sciences of the United States of America. 1990, Vol 87, Num 20, pp 8056-8059, issn 0027-8424, 4 p.Article

MAR, a novel high-incidence Rh antigen revealing the existence of an allelic sub-system including CW (Rh8) and CX (Rh9) with exceptional distribution in the Finnish populationSISTONEN, P; SARENEVA, H; PIRKOLA, A et al.Vox sanguinis (Basel. 1956). 1994, Vol 66, Num 4, pp 287-292, issn 0042-9007Article

DiDistribution of blood groups in the East African Somali populationSISTONEN, P; KOISTINEN, J; ADEN ABDULLE, O et al.Human heredity. 1987, Vol 37, Num 5, pp 300-313, issn 0001-5652Article

Molecular heterogeneity of the Jknull phenotype : expression analysis of the Jk(S291P) mutation found in finnsSIDOUX-WALTER, F; LUCIEN, N; NISSINEN, R et al.Blood. 2000, Vol 96, Num 4, pp 1566-1573, issn 0006-4971Article

Age and origin of two common MLH1 mutations predisposing to hereditary colon cancerMOISIO, A.-L; SISTONEN, P; WEISSENBACH, J et al.American journal of human genetics. 1996, Vol 59, Num 6, pp 1243-1251, issn 0002-9297Article

Clues to the pathogenesis of familial colorectal cancerAALTONEN, L. A; PELTOMÄKI, P; PETERSEN, G. M et al.Science (Washington, D.C.). 1993, Vol 260, Num 5109, pp 812-816, issn 0036-8075Article

Points mutations characterize KEL10, the KEL3, KEL4, and KEL21 alleles, and the KEL17 and KEL11 allelesLEE, S; WU, X; SON, S et al.Transfusion (Philadelphia, PA). 1996, Vol 36, Num 6, pp 490-494, issn 0041-1132Article

Duplication of exon 3 in the glycophorin C gene gives rise to the Ls4a blood group antigenREID, M. E; MAWBY, W; KING, M.-J et al.Transfusion (Philadelphia, PA). 1994, Vol 34, Num 11, pp 966-969, issn 0041-1132Article

Genetic mapping of the erythropoietin receptor geneSISTONEN, P; TRÄSKELIN, A.-L; LEHVÄSLAIHO, H et al.Human genetics. 1993, Vol 92, Num 3, pp 299-301, issn 0340-6717Article

A linkage map spanning the locus for diastrophic dysplasia (DTD)HÄSTBACKA, J; SISTONEN, P; KAITILA, I et al.Genomics (San Diego, Calif.). 1991, Vol 11, Num 4, pp 968-973, issn 0888-7543Article

Terminology for red cell surface antigensDANIELS, G. L; ANSTEE, D. J; LOMAS-FRANCIS, C et al.Vox sanguinis (Basel. 1956). 1999, Vol 77, Num 1, pp 52-57, issn 0042-9007Article

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