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Results 1 to 25 of 5171

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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

Robust method for distinguishing heterozygous from homozygous transgenic alleles by multiplex ligation-dependent probe assayKOZLOWSKI, Piotr; MEI LIN; MEIKLE, Lynsey et al.BioTechniques. 2007, Vol 42, Num 5, issn 0736-6205, 584-588 [3 p.]Article

Novel NR2E3 mutations (R104Q, R334G) associated with a mild form of enhanced s-cone syndrome demonstrate compound heterozygosityHAYASHI, Takaaki; GEKKA, Tamaki; GOTO-OMOTO, Satoshi et al.Ophthalmology (Rochester, MN). 2005, Vol 112, Num 12, pp 2115-2122, issn 0161-6420, 8 p.Article

Atypical mild enhanced S-cone syndrome with novel compound heterozygosity of the NR2E3 geneLAM, Byron L; GOLDBERG, Jeffrey L; HARTLEY, Kristen L et al.American journal of ophthalmology. 2007, Vol 144, Num 1, pp 157-159, issn 0002-9394, 3 p.Article

Expected levels of heterozygosity in autotetraploid progeny populationsMCELROY, A. R.Euphytica. 1991, Vol 55, Num 2, pp 117-123, issn 0014-2336Article

Bleeding symptoms in carriers of hemophilia A and BBUNSCHOTEN, E. P. M; VAN HOUWELINGEN, J. C; SJAMSOEDIN VISSER, E. J. M et al.Thrombosis and haemostasis. 1988, Vol 59, Num 3, pp 349-352, issn 0340-6245Article

Heterozygous manifestations of Langer mesomelic dysplasiaGOLDBLATT, J; WALLIS, C; VILJOEN, D et al.Clinical genetics. 1987, Vol 31, Num 1, pp 19-24, issn 0009-9163Article

Compound heterozygosity involving Antithrombin Cambridge II (p.Ala416Ser) in antithrombin deficiencyAGUILA, Sonia; MARTINEZ-MARTINEZ, Irene; VICENTE, Vicente et al.Thrombosis and haemostasis. 2013, Vol 109, Num 3, pp 556-558, issn 0340-6245, 3 p.Article

Heterozygous missense mutations in SMARCA2 cause Nicolaides-Baraitser syndromeVAN HOUDT, Jeroen K. J; NOWAKOWSKA, Beata Anna; CASTORI, Marco et al.Nature genetics. 2012, Vol 44, Num 4, pp 445-449, issn 1061-4036, 5 p.Article

Heterozygosity in apomictic organismsPAMILO, P.Hereditas (Landskrona). 1987, Vol 107, Num 1, pp 95-101, issn 0018-0661Article

Absence of thrombosis in subjets with heterozygous protein C deficiencyMILETICH, J; SHERMAN, L; BROZE, G. JR et al.The New England journal of medicine. 1987, Vol 317, Num 16, pp 991-996, issn 0028-4793Article

Hb Lepore-Hb C and Hb Lepore-β0-thalassemia compound heterozygotes in an algerian familyFRANCINA, A; DORLEAC, E; AUBRY, M et al.Hemoglobin. 1985, Vol 9, Num 5, pp 505-508, issn 0363-0269Article

Two-hit model for progression of medulloblastoma preneoplasia in Patched heterozygous micePAZZAGLIA, S; TANORI, M; GIANGASPERO, F et al.Oncogene (Basingstoke). 2006, Vol 25, Num 40, pp 5575-5580, issn 0950-9232, 6 p.Article

Haldane's rule has multiple genetic causesORR, H. A.Nature (London). 1993, Vol 361, Num 6412, pp 532-533, issn 0028-0836Article

Fetal hemoglobin in normal adults and β-thalassemia heterozygotesKUTLAR, A; KUTLAR, F; LI-GHAO GU et al.Human genetics. 1990, Vol 85, Num 1, pp 106-110, issn 0340-6717, 5 p.Article

Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNVJARUPON FAH SATHIRAPONGSASUTI; LEE, Hane; HORST, Basil A. J et al.Bioinformatics (Oxford. Print). 2011, Vol 27, Num 19, pp 2648-2654, issn 1367-4803, 7 p.Article

Absence of allelic loss on chromosome 5q by RFLP analysis in preleukemiaSHEPHERD, L; CAMERON, C; GALBRAITH, P et al.Leukemia research. 1991, Vol 15, Num 5, pp 297-303, issn 0145-2126Article

Spectrin Tunis (α1/78): a new αI variant that causes asymptomatic hereditary elliptocytosis in the heterozygous stateMORLE, L; ALLOISIO, N; DUCLUZEAU, M. T et al.Blood. 1988, Vol 71, Num 2, pp 508-511, issn 0006-4971Article

Clonal inheritance in parthenogenetic whiptail lizards: biochemical evidenceDESSAUER, H. C; COLE, C. J.The journal of heredity. 1986, Vol 77, Num 1, pp 8-12, issn 0022-1503Article

Developmental stability of rainbow trout hybrids: genomic coadaptation or heterozygosity?FERGUSON, M. M.Evolution. 1986, Vol 40, Num 2, pp 323-330, issn 0014-3820Article

Hb A-like sickle haemoglobin: Hb S-ProvidenceGALE, R. E; BLAIR, N. E; HUEHNS, E. R et al.British journal of haematology. 1988, Vol 70, Num 2, pp 251-252, issn 0007-1048Article

Pulmonary function in obligate heterozygotes for cystic fibrosisBYARD, P. J; DAVIS, P. B.The American review of respiratory disease. 1988, Vol 138, Num 2, pp 312-316, issn 0003-0805Article

Genetic recombination between closely linked markers of bacteriophage T4. II: A mutation which reduces the formation of heteroduplex heterozygotesHONDA, M.Japanese journal of experimental medicine. 1986, Vol 56, Num 6, pp 309-314, issn 0021-5031Article

Genetics of Glossina morsitans morsitans (Diptera: Glossinidae). XII: Comparison of field-collected and laboratory-reared fliesGOODING, R. H; JORDAN, A. M.Canadian journal of genetics and cytology. 1986, Vol 28, Num 6, pp 1016-1021, issn 0008-4093Article

Les individus inégaux devant les risques infectieuxANDUJAR, Gauthier.Biofutur (Puteaux). 2007, Num 277, pp 11-11, issn 0294-3506, 1 p.Article

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