نتایج جستجو برای: iranian families

تعداد نتایج: 162129  

Journal: :iranian journal of public health 0
mr nikbakhtzadeh s tirgari

field collection in nahavand county (hamedan province, iran) revealed 9 blister beetle (col: meloidae) species from three different tribes of subfamily meloinae. in tribe mylabrini, mylabris impressa chevrolat 1837, mylabris schreibersi reiche 1865, mylabris variabilis (pallas, 1781), mylabris guerini chevrolat 1837, lydoceras bilineatus thomas 1897 and croscherichia spp. pardo alcaide identifi...

Journal: :genetics in the 3rd millennium 0
hossein najmabadi mojgan babanejad maryam beheshtian fariba ardalani hossein daghagh nooshin nikzat

hearing loss (hl) is the most common communication disorder affecting about 1/1000 births worldwide caused by environmental or genetic factors. about 30-50% is attributed to genetic factors and till now more than 85 genes have been implicated in non-syndromic hl. in iran, hl is second to intellectual disability as the most common disability, affecting 1 of every 166 persons. about 15 years ago ...

G. H. Vosoughi K. Gharra M. Noorinejad M. R. Fatemi M. Rabbaniha, S. Jamili

  Khark and Kharko Islands are located at far northern point of fringing coral reefs in the Iranian coast of the Persian Gulf. These coralline are the habitats of the wildlife refuge with total area of 2400ha and located in the territory of Bushehr province. The present study was carried out from July 2006 to June 2007 over 12 stations. Sampling was conducted obliquely from bottom using Bongo-n...

Journal: :JASIST 2008
Farideh Osareh Katherine W. McCain

To study the structure of Iranian chemistry research, we identified 43 Iranian and international chemists who were highly cited in 7,682 Iranian chemistry publications (defined as an article with at least one Iranian author address) indexed in Science Citation Index (SciSearch) between 1990 and 2006, inclusive. We collected cocitation data for these authors from the entire SciSearch file (Dialo...

Journal: :iranian journal of public health 0
p ghandil dd farhud s zeinali a ghadiri

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...

G. H. Vosoughi, K. Gharra, M. Noorinejad, M. R. Fatemi, M. Rabbaniha, S. Jamili,

  Khark and Kharko Islands are located at far northern point of fringing coral reefs in the Iranian coast of the Persian Gulf. These coralline are the habitats of the wildlife refuge with total area of 2400ha and located in the territory of Bushehr province. The present study was carried out from July 2006 to June 2007 over 12 stations. Sampling was conducted obliquely from bottom using Bongo-n...

Journal: :Child development 1998
A Kalil J S Eccles

Recent welfare reform legislation requires increased parental work effort and imposes time limits on the receipt of federal assistance. These changes were based in part on assumptions that parental welfare receipt may be negatively related to family processes and children's attitudes and behaviors. Currently, researchers know little about the effects of welfare by itself relative to the effects...

1997
Thomas Kaplan

In August 1996, Congress and the president replaced the 60-year-old Aid to Families with Dependent Children (AFDC) program with a block grant, Temporary Assistance to Needy Families (TANF), permitting states to experiment with new forms of assistance to low-income families. States seem likely to try increasingly ambitious reforms as they gain experience under their TANF flexibility, at least if...

Mutations in the connexin 26 (Cx26) gene at the DFNB1 locus on chromosome 13q12 are associated with autosomal recessive non-syndromic hearing loss (ARNSHL). There are many known mutations in this gene that cause hearing loss. A single frameshift, at position 35 (35delG) accounts for 50% of mutations in the Caucasian population with carrier frequencies of 1.5-2.5%. In this study we investigated ...

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