To modeling of Suitability Iranian Oak site to establish coppice regenerations, chahartagh forest reserve, Ardal region, chaharmehal and Bakhtiari Province, southern Zagros forest, and southwest Iranian state was selected. To modeling Suitability Iranian Oak used the physiographic element, soil depth, climatology and distance from village selected. To this study used the raster formats by pixel...

the data set used in this study contained 8793 records of lamb's longevity (days) from 320 sires and 2349 dams collected during 1989 to 2014, from the lori-bakhtiari flock at shooli station in shahrekord, iran. genetic parameters (partitioned into autosomal, sex-linked and maternal) and breeding values of cumulative lamb's longevity from birth up to yearling age (at 1, 2, 3, 6, 9 and ...

the length-weight relationships for three fish species from beheshtabad river, karun river drainage (western chaharmahal and bakhtiari provinces, iran) were investigated. the values of the slope parameter ( b ) in the length-weight relationship equations were determined as 2.79 for capoeta damascina , 3.10 for chondrostoma regium and 3.09 for oncorhynchus mykiss , all of which were significantl...

Identification of Problems faced by Graduates of Farhangian University Campuses in Chaharmahal and Bakhtiari Province   J. Torkzaadeh, Ph.D.* M. Saadeghiaan Sooraki** R. Marzooghi, Ph.D.*** J. Jahaani, Ph.D.****   To improve any learning environment, its problems need to be identified. To do so at the Farhangian University campuses in the province of Chaharmahal and Bakhtiari Province,...

Introduction: Congenital hypothyroidism (CH) is one of the most common endocrine and metabolic disorders a preventable cause mental retardation across world. This disorder can be prevented if diagnosed treated before age four weeks. Objectives: study was performed to investigate incidence rate CH in infants Chaharmahal Bakhtiari province. Patients Methods: The data this were obtained by screeni...

Dear Editor, Beta Thalassemia major is a genetic disease with an autosomal recessive pattern and is differentiated by severe microcytic hypochromic hemolytic anemia with hepatosplenomegaly, ineffective erythropoiesis and bone marrow expansion. The β-globin (HBB) gene coding for β-chain expression is located on a 50 kb globin gene cluster on the short arm of chromosome 11, whose mutation mediate...