نتایج جستجو برای: new mutation
تعداد نتایج: 2104375 فیلتر نتایج به سال:
In this paper, a new genetic algorithm (GA) is presented for solving the multi-mode resource-constrained project scheduling problem (MRCPSP) with minimization of project makespan as the objective subject to resource and precedence constraints. A random key and the related mode list (ML) representation scheme are used as encoding schemes and the multi-mode serial schedule generation scheme (MSSG...
Harlequin Ichthyosis (HI) describes a severe erythrodermic ichthyosis and causes a distinctive and grotesque appearance at birth. Survival is now possible therefore, harlequin ichthyosis is a more appropriate term than harlequin fetus. Incidence is 1 in 300,000 births. An autosomal recessive pattern of inheritance is seen in this disorder, but a new autosomal dominant mutation may possibly ...
A 10-month-old female presented with severe progressive wedge-shaped thickening and discoloration of all twenty nails. Further evaluations revealed palmoplantar keratoderma along with recurrent acral blisters causing residual crusted ulcers which were present during the past six months. Other findings include scalp kinky hair and dental caries. Patient history was remarkable for natal tee...
experience of double revolutionary upheavals in russia during the 20th century which produced a new socio-economic regularity on one hand and changed the political system from monarchial to democratic republic and then soviet state and finally presidential republic at the end of 20th century on the other hand are treated as democratic movements. in this regard, crumbling of ex-soviet regime and...
Background Myeloproliferative disorders are a group of diseases characterized by increased proliferation of myeloid lineage. In addition to JAK2V617F mutation, several mutations in the c-MPL gene were described in patients with Philadelphia-negative chronic myeloproliferative disorders that could be important in the pathogenesis of diseases. The aim of present study was to investigate the fre...
Background : Familial Mediterranean fever (FMF) is an autosomal recessive disease, which is characterized by recurrent short episodes of inflammation in serous membranes. It is most prevalent in Western Mediterranean population. MEFV is the only gene currently known to be associated with this disease. Previous studies revealed that 6% of Iranian Jewish residents in Israel were carriers of MEFV ...
hemophilia b is factor ix deficiency and is inherited as x-linked recessive disorder. the subject of carrier detection in hemophilias has received new impetus in the last several years. analysis of factor ix gene polymorphisms is considered the best approach for prenatal diagnosis and hemophilia b carrier detection, if the identification of the gene mutation is possible. allele frequencies of t...
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