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DIAGNOSIS OF HETEROZYGOUS BETA THALASSAEMIAFRANZINI C.1975; J. CLIN. PATHOL.; G.B.; DA. 1975; VOL. 28; NO 3; PP. 203-204Article

UN NOUVEAU SYSTEME RAPIDE POUR LE DEPISTAGE DE LA DREPANOCYTOSE PAR L'IDENTIFICATION ET LA DIFFERENCIATION DE L'HEMOGLOBINE AA, AS ET SS1973; SEM. HOP., PATHOL. BIOL.; FR.; DA. 1973; VOL. 21; NO 1; PP. 110-111Serial Issue

SINGLE-GENE CONDITIONAL HETEROSIS.KIDWELL JF; WILL C.1974; AMER. NATURALIST; U.S.A.; DA. 1974; VOL. 108; NO 964; PP. 883-888; BIBL. 11REF.Article

DIFFERENTIATION OF IRON DEFICIENCY FROM THALASSAEMIA TRAIT BY ROUTINE BLOOD-COUNT = DIFFERENCIATION DE LA DEFICIENCE DE FER DU THALASSEMIE TRAIT PAR LA NUMERATION GLOBULAIRE ORDINAIRE1973; LANCET; G.B.; DA. 1973; NO 7801; PP. 449-452; BIBL. 8 REF.Serial Issue

HETEROZYGOUS DIPLOID STRAINS OF ASPERGILLUS NIDULANS: ENHANCED VIRULENCE FOR MICE IN COMPARISON TO A PROTOTROPHIC HAPLOID STRAINPURNELL DM; MARTIN GM.1973; MYCOPATHOL. MYCOL. APPL; PAYS-BAS; DA. 1973; VOL. 49; NO 4; PP. 307-319; BIBL. 14REF.Serial Issue

A ROBERTSONIAN TRANSLOCATION IN BRITISH FRIESIAN CATTLEPOLLOCK DL; BOWMAN JC.1974; J. REPRODUCT. FERTIL.; G.B.; DA. 1974; VOL. 40; NO 2; PP. 423-432; H.T. 2; BIBL. 1P.Article

Les populations de Mytilidae de Kerguelen (océan Austral) : génétique et adaptation à l'environnement de Mytilus desolationisBlot, Michel; Soyer, Jacques.1989, 183 p.Thesis

TWO RARE MIXED HETEROZYGOTES FOR THE FLUORIDE VARIANT AND SILENT CHOLINESTERASES = DEUX HETEROZYGOTES MIXTES RARES POUR LA VARIANTE F ET LES CHOLINESTERASES SILENCIEUSESBECKER CE.1972; ANESTHESIOLOGY; U.S.A.; DA. 1972; VOL. 36; NO 5; PP. 513-514; BIBL. 11REF.Serial Issue

A DIELECTRIC INVESTIGATION OF THE WATER OF HYDRATION OF LOW-DENSITY LIPOPROTEINS IN FAMILIAL HYPERBETALIPOPROTEINAEMIA = UNE INVESTIGATION DIELECTRIQUE DE L'EAU D'HYDRATATION DES LIPOPROTEINES DE BASSE DENSITE DANS L'HYPERBETALIPOPROTEINEMIE FAMILIALEGRANT EH; SHEPPARD RJ; MILLS GL et al.1972; LANCET; G.B.; DA. 1972; NO 7761; PP. 1159-1161; BIBL. 16REF.Serial Issue

HEREDITARY TYROSINEMIA: METABOLIC STUDIES IN A PATIENT WITH PARTIAL P-HYDROXYPHENYLPYRUVATE HYDROXYLASE ACTIVITY = TYROSINEMIE HEREDITAIRE: ETUDES METABOLIQUES CHEZ UN MALADE AVEC UNE ACTIVITE PARTIELLE DE LA P-HYDROXYPHENYLPYRUVATE HYDROXYLASE1972; J. PEDIATR.; U.S.A.; DA. 1972; VOL. 80; NO 6; PP. 994-1004; BIBL. 1P.Serial Issue

A POSSIBLE PARTIAL HETEROZYGOTE OF AN INFLUENZA A VIRUSSCHOLTISSEK C; ROHDE W; HARMS E et al.1978; VIROLOGY; USA; DA. 1978; VOL. 89; NO 2; PP. 506-516; BIBL. 25 REF.Article

HEMOGLOBINOPATHIES OF CLINICAL IMPORTANCE = HEMOGLOBINOPATHIES D'IMPORTANCE CLINIQUESCHWARTZ E.1972; PEDIATR. CLIN. N. AMER.; U.S.A.; DA. 1972; VOL. 19; NO 4; PP. 889-905; BIBL. 2 P.Serial Issue

Color discrimination in carriers of color deficiencyHOOD, S. M; MOLLON, J. D; PURVES, L et al.Vision research (Oxford). 2006, Vol 46, Num 18, pp 2894-2900, issn 0042-6989, 7 p.Article

A false single nucleotide polymorphism generated by gene duplication compromises meat traceabilitySANZ, Arianne; ORDOVAS, Laura; ZARAGOZA, Pilar et al.Meat science. 2012, Vol 91, Num 3, pp 347-351, issn 0309-1740, 5 p.Article

Genes made molecularWATERS, C. K.Philosophy of science (East Lansing). 1994, Vol 61, Num 2, pp 163-185, issn 0031-8248Article

The aprt heterozygote/hemizygote sytstem for screening mutagenic agents allows detection of large deletionsBRADLEY, W. E. C; ABDELMAJID BELOUCHI; MESSING, K et al.Mutation research. 1988, Vol 199, Num 1, pp 131-138, issn 0027-5107Article

Changes in disease gene frequency over time with differential genotypic fitness and various control strategiesTHOMPSON, P. N; HEESTERBEEK, J. A. P; VAN ARENDONK, J. A. M et al.Journal of animal science. 2006, Vol 84, Num 10, pp 2629-2635, issn 0021-8812, 7 p.Article

Iron absorption in male C282Y heterozygotesROE, Mark A; HEATH, Anne-Louise M; OYSTON, Sarah L et al.The American journal of clinical nutrition. 2005, Vol 81, Num 4, pp 814-821, issn 0002-9165, 8 p.Article

Heterozygote Genotypes at rs2222823 and rs2811712 SNP Loci are Associated with Cerebral Small Vessel Disease in Han Chinese PopulationWEI LI; BO HU; LIAO, Xiao-Ling et al.CNS neuroscience & therapeutics (Print). 2012, Vol 18, Num 7, pp 558-565, issn 1755-5930, 8 p.Article

16q-linked autosomal dominant cerebellar ataxia : A clinical and genetic studyOUYANG, Y; SAKOE, K; AMINO, T et al.Journal of the neurological sciences. 2006, Vol 247, Num 2, pp 180-186, issn 0022-510X, 7 p.Article

New Intermediate Phenotype Between MED and DD Caused by Compound Heterozygous Mutations in the DTDST GeneCZARNY-RATAJCZAK, Malwina; BIEGANSKI, Tadeusz; ROGALA, Piotr et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 12, pp 3036-3042, issn 1552-4825, 7 p.Article

A novel compound heterozygous mutation in the DAP12 gene in a patient with Nasu-Hakola diseaseKURODA, Ryo; SATOH, Junichi; YAMAMURA, Takashi et al.Journal of the neurological sciences. 2007, Vol 252, Num 1, pp 88-91, issn 0022-510X, 4 p.Article

Untersuchungen zum Heterosis-Effekt bei Neugeborenen = Researches on heterosis effects in newbornsSCHMIDT, H. D; GLAVCE, C; WISCHER, S et al.Anthropologischer Anzeiger. 1996, Vol 54, Num 2, pp 125-134, issn 0003-5548Article

Screening for co-existence of α-thalassemia in β-thalassemia and in HbE heterozygotes via an enzyme-linked immunosorbent assay for Hb Bart's and embryonic ζ-globin chainTATU, Thanusak; KIEWKARNKHA, Tiemjan; KHUNTARAK, Surakit et al.International journal of hematology. 2012, Vol 95, Num 4, pp 386-393, issn 0925-5710, 8 p.Article

Effet de stratification et structure génétique d'une population : Les Dogon de Sangha (Mali) = Stratification effect and a population's genetic structure : The Dogon from Sangha (Malia)BELLIS, G; KRISHNAMOORTHY, R; NAGEL, R. L et al.Population. 1996, Vol 51, Num 2, pp 482-487, issn 0032-4663Article

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