نتایج جستجو برای: genetics

تعداد نتایج: 76572  

Journal: :Annual Review of Genetics 2017

بینافر, سیما, مهدیه, نجات,

Background and purpose: Phenylketonuria (PKU), a genetic disorder with an autosomal recessive pattern of inheritance, is mainly due to phenyalanine hydroxylase deficiency. In Iran, many studies have investigated the genetics of this disease among different populations. This study aimed to report the frequencies of the mutations for each population as determined in different studies. Material...

Journal: :genetics in the 3rd millennium 0
محمد حسن کریمی نژاد mohammad hassan kariminejad

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Journal: :genetics in the 3rd millennium 0
محمد حسن کریمی نژاد mohammad hassan kariminejad

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Journal: :بینا 0
توکا بنایی t banaei مشهد- بلوار شهید قره نی- بیمارستان چشم پزشکی خاتم الانبیاء (ص)- مرکز تحقیقات چشم داریوش فرخ تهرانی d farrokh tehrani مشهد- بلوار شهید قره نی- بیمارستان چشم پزشکی خاتم الانبیاء (ص)- مرکز تحقیقات چشم محمدرضا عباس زادگان mr abbaszadegan مشهد- بلوار شهید قره نی- بیمارستان چشم پزشکی خاتم الانبیاء (ص)- مرکز تحقیقات چشم

age-related macular degeneration (amd) is the leading cause of blindness in old subjects. it is a multifactorial disease with both environmental and genetic factors playing some role in its pathogenesis. similar to many other genetic diseases, the inheritance pattern of amd does not fit into simple mendelian rules. these diseases are caused by the presence of multiple genetic factors and are ca...

Journal: :iranian journal of neonatology 0
amin khaleghparast m.sc. of biology-genetics, tehran science and research branch of islamic azad university, tehran, iran sharif khaleghparast b.eng. of industrial engineering, iran university of science and technology (iust), tehran, iran hossein khaleghparast ph.d. of public law, tehran science and research branch of islamic azad university, tehran, iran

introduction: one factor known to cause thrombophilia in women with unexplained recurrent spontaneous abortion (rsa) is c677t polymorphism of methylenetetrahydrofolate reductase gene. this study aimed to determine the association between rsa and mthfr c677t polymorphism in iranian patients. methods: in this case-control study, 30 patients with previous history of two or more consecutive unexpla...

Journal: :journal of research in health sciences 0
hamid pour-jafari morteza hashemzadeh chaleshtari mohammad reza imani

background: determining of gene frequencies of a, band 0 genes from abo blood group system and d and d genes from rhesus system are objectives of the present study. methods: the study was a cross sectional descriptive study. all the voluntary blood donors, 7361 people, attending to the hamadan, iran, blood bank during 1996 were studied. primary information from the sex of blood donors and their...

Journal: :iranian journal of public health 0
h pour-jafari dd farhud

workers of operating rooms in hospitals are chronically in exposure to rather higher dose of chemicals, e.g. halothane and nitrous oxide, than general population. concern that exposure to waste anesthetic gases may cause mutagenic, carcinogenic, or teratogenic changes has provided the impetus for many recent studies. the goal of present work was to determine incidence of the fetal deaths and se...

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