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Impact of heterozygous c.657-661del, p.I171V and p.R215W mutations in NBN on nibrin functionsDZIKIEWICZ-KRAWCZYK, Agnieszka; MOSOR, Maria; JANUSZKIEWICZ, Danuta et al.Mutagenesis. 2012, Vol 27, Num 3, pp 337-343, issn 0267-8357, 7 p.Article

Phenotypic effects of heterozygosity for a BRCA2 mutationWARREN, Madhuri; LORD, Christopher J; MASABANDA, Julio et al.Human molecular genetics (Print). 2003, Vol 12, Num 20, pp 2645-2656, issn 0964-6906, 12 p.Article

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

Heterozygote excess is repeatedly observed in females at the BRCA2 locus N372HTEARE, M. D; COX, A; SHORTO, J et al.Journal of medical genetics. 2004, Vol 41, Num 7, pp 523-528, issn 0022-2593, 6 p.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

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

Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressureFAVA, C; MONTAGNANA, M; AURELL, M et al.Human molecular genetics (Print). 2008, Vol 17, Num 3, pp 413-418, issn 0964-6906, 6 p.Article

Distribution of familial nephritis antigen in normal tissue and renal basement membranes of patients with homozygous and heterozygous Alport familial nephritis: relationship of familial nephritis and goodpasture antigens to novel collagen chains and type IV collagenKLEPPEL, M. M; KASHTAN, C; SANTI, P. A et al.Laboratory investigation. 1989, Vol 61, Num 3, pp 278-289, issn 0023-6837, 12 p.Article

Sampling variance of the genetic diversity indexQIFA ZHANG; ALLARD, R. W.The journal of heredity. 1986, Vol 77, Num 1, pp 54-55, issn 0022-1503Article

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

Loss of heterozygosity and its correlation with expression profiles in subclasses of invasive breast cancersWANG, Zhigang C; MING LIN; IGLEHART, James D et al.Cancer research (Baltimore). 2004, Vol 64, Num 1, pp 64-71, issn 0008-5472, 8 p.Article

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

Assessment of chronic γ radiosensitivity as an in vitro assay for heterozygote identification of ataxia-telangiectasiaWEEKS, D. E; PATERSON, M. C; LANGE, K et al.Radiation research. 1991, Vol 128, Num 1, pp 90-99, issn 0033-7587Article

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