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Results 1 to 25 of 4471

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Thalassemia minor: routine erythrocyte measurements and differentiation from iron deficiencyJOHNSON, C. S; TEGOS, C; BEUTLER, E et al.American journal of clinical pathology. 1983, Vol 80, Num 1, pp 31-36, issn 0002-9173Article

Detection of haemophilia carriers: multivariate analysis compared with discriminant analysis using up to five factor VIII variatesDUNCAN, B. M; TUNBRIDGE, L. J; DUNCAN, E. M et al.British journal of haematology. 1984, Vol 57, Num 1, pp 113-121, issn 0007-1048Article

Two new cases of heterozygosity for hemoglobin Knossos α2β2 27 Ala→Ser detected in the French West Indies and AlgeriaGALACTEROS, F; GARIN, J. D; ROSA, J et al.Hemoglobin. 1984, Vol 8, Num 3, pp 215-228, issn 0363-0269Article

Reliability of the Tønnesen technique for the identification of Hunter carriersPETRUSCHKA, L; MACHILL, G; WEHNERT, M et al.Human genetics. 1983, Vol 64, Num 4, pp 404-406, issn 0340-6717Article

Hemoglobin C in heterozygote carriersCAMERON, B. F; SMITH, D. B; CODY, B et al.American journal of hematology. 1984, Vol 17, Num 4, pp 437-438, issn 0361-8609Article

Double heterozygosity for hemoglobins C and Lepore in an American black manSCHOENTAG, R; PEDERSEN, J; BALLARD, H et al.Archives of pathology & laboratory medicine (1976). 1985, Vol 109, Num 8, pp 777-779, issn 0363-0153Article

Hemoglobin constitution of double heterozygotes for α or β-thalassemia and HB J SardegnaMACCIONI, L; GALANELLO, R; MELIS, M. A et al.Hemoglobin. 1984, Vol 8, Num 5, pp 497-507, issn 0363-0269Article

Phenotypic effect of heterozygous #7B-A and #7B-B°-thalassemia interactionMELIS, M. A; PIRASTU, M; GALANELLO, R et al.Blood. 1983, Vol 62, Num 1, pp 226-229, issn 0006-4971Article

Heterozygosity and developmental stability in gynogenetic diploid and triploid rainbow troutLEARY, R. F; ALLENDORF, F. W; KNUDSEN, K. L et al.Heredity (Edinburgh. Print). 1985, Vol 54, Num 2, pp 219-225, issn 0018-067XArticle

Etude expérimentale des relations entre mode de reproduction et hétérozygotie individuelle chez Daphnia magnaBARAUSKENE, V. K; LEKYAVICHYUS, EH. K; ALTUKHOV, YU. P et al.Genetika. 1985, Vol 21, Num 4, pp 591-598, issn 0016-6758Article

Heterozygous β-thalassemia in pregnancyCOOLEY, J. R; KITAY, D. Z.Journal of reproductive medicine. 1984, Vol 29, Num 2, pp 141-142, issn 0024-7758Article

Carrier detection in Hunter syndromeARCHER, I. M; YOUNG, I. D; REES, D. W et al.American journal of medical genetics. 1983, Vol 16, Num 1, pp 61-69, issn 0148-7299Article

Reliability of the use of fructose 1-phosphate to detect Hunter cells in fibroblast-cultures of obligate carriers of the Hunter syndromeTONNESEN, T; GÜTTLER, F; LYKKELUND, C et al.Human genetics. 1983, Vol 64, Num 4, pp 371-375, issn 0340-6717Article

The sicca syndrome in thalassaemia majorBORGNA-PIGNATTI, C; CAMMARERI, V; DE STEFANO, P et al.British medical journal (1857). 1984, Vol 288, Num 6418, pp 668-669, issn 0007-1447Article

Testing genotype frequencies and heterozygositiesPAMILO, P; VARVIO-AHO, S.Marine biology (Berlin). 1984, Vol 79, Num 1, pp 99-100, issn 0025-3162Article

Partial inbreeding: equilibrium heterozygosity and the heterozygosity paradoxHEDRICK, P. W; COCKERHAM, C. C.Evolution. 1986, Vol 40, Num 4, pp 856-861, issn 0014-3820Article

Prescreening of beta-thalassaemia carriers: a comparison between Bayesian and other approachesSTEVE, G; ROSSI-MORI, A.Statistician (London. Print). 1983, Vol 32, Num 1-2, pp 233-239, issn 0039-0526Article

α-Thalassemia trait with the ααα/-genotype in a chineseZHANG JUN-WU; WU GUAN-YUN; YANG XUE-YONG et al.Hemoglobin. 1984, Vol 8, Num 2, pp 183-187, issn 0363-0269Article

The prevalence of heterozygotes for α-mannosidosis in populations of Augus galloway and Murray grey cattle in New South WalesHEALY, P. J.Génétique, sélection, évolution. 1983, Vol 15, Num 3, pp 455-459Article

HEMOPHILIA AND THE FEMALE: CONSIDERATIONS FOR THE RADIOLOGISTHELLER RM; ROLOFF JS; KIRCHNER SG et al.1979; RADIOLOGY; USA; DA. 1979; VOL. 133; NO 3; PP. 601-603; BIBL. 29 REF.Article

Bêtathalassémie hétérozygote sans microcytose = Heterozygous beta-thalassaemia without microcytosisGALLIEN, N; MAIER-REDELSPERGER, M; ROTHSCHILD, E et al.La Presse médicale (1983). 1988, Vol 17, Num 30, issn 0755-4982, 1538Article

Carrier detection in the hemophiliasLILLICRAP, D. P; WHITE, B. N; HOLDEN, J. J. A et al.American journal of hematology. 1987, Vol 26, Num 3, pp 285-296, issn 0361-8609Article

Carrier detection and X-inactivation studies in the fragile X syndrome. Cytogenetic studies in 63 obligate and potential carriers of the fragile XBRONDUM NIELSEN, K; TOMMERUP, N; POULSEN, H et al.Human genetics. 1983, Vol 64, Num 3, pp 240-245, issn 0340-6717Article

Extramedullary hematopoiesis presenting as a pelvic mass in a patient with β-thalassemia intermediaNEWTON, K. L; MCNEELEY, G. JR; NOVICK, M et al.JAMA, the journal of the American Medical Association. 1983, Vol 250, Num 16, pp 2178-2179, issn 0098-7484Article

Existence of polymorphic genotypic equilibria under asymmetry of homozygotic disadvantage and a deficiency of heterozygotesZIEHE, M.Heredity (Edinburgh. Print). 1984, Vol 52, pp 337-346, issn 0018-067X, 3Article

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