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

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

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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

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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

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

Circulating microparticles are elevated in carriers of Factor V LeidenENJETI, Anoop K; LINCZ, Lisa F; SCORGIE, Fiona E et al.Thrombosis research. 2010, Vol 126, Num 3, pp 250-253, issn 0049-3848, 4 p.Article

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

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

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

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

Exploring efferent-mediated DPOAE adaptation in three different guinea pig strainsSKJÖNSBERG, Asa; HALSEY, Kärin; ULFENDAHL, Mats et al.Hearing research. 2007, Vol 224, Num 1-2, pp 27-33, issn 0378-5955, 7 p.Article

Mitotic delay in lymphocytes from BRCA1 heterozygotes unable to reduce the radiation-induced chromosomal damageFEBRER, Emma; MESTRES, Marta; CABALLIN, Maria Rosa et al.DNA repair. 2008, Vol 7, Num 11, pp 1907-1911, issn 1568-7864, 5 p.Article

The role of ATM in breast cancer developmentPROKOPCOVA, Jana; KLEIBI, Zdenek; BANWELL, Claire M et al.Breast cancer research and treatment. 2007, Vol 104, Num 2, pp 121-128, issn 0167-6806, 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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Sex-related differences in chromatic sensitivityRODRIGUEZ-CARMONA, M; SHARPE, L. T; HARLOW, J. A et al.Visual neuroscience (Print). 2008, Vol 25, Num 3, pp 433-440, issn 0952-5238, 8 p.Conference Paper

Poorer color discrimination by females when tested with pseudoisochromatic plates containing vanishing designs on neutral backgroundsBARAAS, Rigmor C.Visual neuroscience (Print). 2008, Vol 25, Num 3, pp 501-505, issn 0952-5238, 5 p.Conference Paper

A,B blood group antigens in tissues of AB heterozygotes : emphasis on normal and neoplastic urotheliumLIMAS, C.The American journal of pathology. 1990, Vol 137, Num 5, pp 1157-1162, issn 0002-9440Article

Audiometric evaluation of carriers of the connexin 26 mutation 35delGFRANZE, Annamaria; CARAVELLI, Antonella; DI LEVA, Francesca et al.European archives of oto-rhino-laryngology. 2005, Vol 262, Num 11, pp 921-924, issn 0937-4477, 4 p.Article

Effect of family history on disclosure patterns of cystic fibrosis carrier statusORMOND, Kelly E; MILLS, Patti L; LESTER, Lucille A et al.American journal of medical genetics. 2003, Vol 119c, Num 1, pp 70-77, issn 0148-7299, 8 p.Conference Paper

Maximal γ-globin expression in the compound heterozygous state for -175 ^Gγ HPFH and β°39 nonsense thalassaemia : a case studyPISTIDDA, P; FROGHERI, L; GUISO, L et al.European journal of haematology. 1997, Vol 58, Num 5, pp 320-325, issn 0902-4441Article

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