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Experimental evaluation of SDL and One-Op mutation for C
(IEEE Computer SocietyCleveland, Ohio, 2014-03-31)
Mutation analysis modifies a program by applying
syntactic rules, called mutation operators, systematically to create
many versions of the program (mutants) that differ in small
ways. Testers then design tests to cause ...
Designing deletion mutation operators
(IEEE Computer SocietyCleveland, Ohio, 2014-03-31)
Mutation analysis modifies a program by applying
syntactic rules, called mutation operators, systematically to create
many versions of the program (mutants) that differ in small
ways. Testers then design tests to cause ...
Analysis of HFE and non-HFE gene mutations in Brazilian patients with hemochromatosis
(Faculdade de Medicina / USP, 2009)
BACKGROUND: Approximately one-half of Brazilian patients with hereditary hemochromatosis (HH) are neither homozygous for the C282Y mutation nor compound heterozygous for the H63D and C282Y mutations that are associated ...
The frequency of 844ins68 mutation in the cystathionine beta-synthase gene is not increased in patients with venous thrombosis
(Ferrata Storti Foundation, 1998-11-01)
Background and Objectives. A frequent mutation in the cystathionine beta-synthase (CBS) gene (844ins68, a 68-bp insertion in the coding region of exon 8) was recently discovered. In the present study we Investigated this ...
Use of the q-Gaussian mutation in evolutionary algorithms
(SPRINGER, 2011)
This paper proposes the use of the q-Gaussian mutation with self-adaptation of the shape of the mutation distribution in evolutionary algorithms. The shape of the q-Gaussian mutation distribution is controlled by a real ...
Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly
(Elsevier B.V., 2010-03-01)
Holoprosencephaly (HPE) is a malformation sequence where the cerebral hemispheres fail to separate into distinct left and right halves. It can be associated with midline structural anomalies of the central nervous system ...
Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly
(Elsevier B.V., 2010-03-01)
Holoprosencephaly (HPE) is a malformation sequence where the cerebral hemispheres fail to separate into distinct left and right halves. It can be associated with midline structural anomalies of the central nervous system ...
The frequency of 844ins68 mutation in the cystathionine β-synthase gene is not increased in patients with venous thrombosis
(1998-11-01)
Background and Objectives. A frequent mutation in the cystathionine β- synthase (CBS) gene (844ins68, a 68-bp insertion in the coding region of exon 8) was recently discovered. In the present study we investigated this ...
Presence of the R1748X mutation in the NF1 gene in a Brazilian patient with ectropion uveae
(Karger, 2004-01-01)
Congenital ectropion uveae is a rare, nonprogressive anomaly characterized by the presence of iris pigment epithelium on the anterior surface of the iris stroma and is occasionally associated with Rieger's anomaly, ...
Presence of the R1748X mutation in the NF1 gene in a Brazilian patient with ectropion uveae
(Karger, 2004-01-01)
Congenital ectropion uveae is a rare, nonprogressive anomaly characterized by the presence of iris pigment epithelium on the anterior surface of the iris stroma and is occasionally associated with Rieger's anomaly, ...