نتایج جستجو برای: genetic diagnosis

تعداد نتایج: 1054612  

Journal: :journal of comprehensive pediatrics 0
mahsa motavaf department of genetics, tarbiat modares university, tehran, ir iran majid sadeghizadeh department of genetics, tarbiat modares university, tehran, ir iran; department of genetics, faculty of biological sciences, tarbiat modares university, p. o. box: 14115-175, tehran, ir iran. tel: +98-2182884409, fax: +98-2182883463سازمان اصلی تایید شده: دانشگاه تربیت مدرس (tarbiat modares university)

context prenatal testing aims to identify fetal chromosomal and genetic disorders prior to delivery. current invasive procedures such as amniocentesis and chorionic villus sampling (cvs) pose a risk to mother and fetus and such diagnostic procedures are available only to high-risk pregnancies, which limits aneuploidy detection rate. the identification of cell-free fetal dna (cffdna) in maternal ...

Journal: :journal of ai and data mining 2015
a. ghaffari s. nobahary

wireless sensor networks (wsns) consist of a large number of sensor nodes which are capable of sensing different environmental phenomena and sending the collected data to the base station or sink. since sensor nodes are made of cheap components and are deployed in remote and uncontrolled environments, they are prone to failure; thus, maintaining a network with its proper functions even when und...

Journal: :genetics in the 3rd millennium 0
امید آریانی omid ariani special medical center, tehran, iran مسعود هوشمند masoud houshmand محمد حسین صنعتی mohammad hossein sanati

wilson disease is a disorder of copper metabolism that can present with hepatic, neurologic, or psychiatric disturbances, or a combination of these, in individuals ranging from age three years to over 50 years. the primary consequence for most of those with wd is liver disease, appearing in late childhood or early adolescence as acute hepatitis, liver failure, or progressive chronic liver disea...

Journal: :Nihon Naika Gakkai Zasshi 2008

Journal: :Ophthalmology Research: An International Journal 2020

Farhud, Daryoush, Pourkalhor, Haniyeh,

Prenatal Diagnosis is the most reliable way of preventing genetic diseases that has been implicated in many countries and has prevented the birth of newborns with different hereditary, congenital and genetic diseases during the past few years. Prenatal diagnosis is actually the use of various diagnostic methods to check the condition of the fetus during pregnancy, because postnatal genetic diso...

Journal: :iranian biomedical journal 0
رامین رادپور ramin radpour مینا رضایی mina rezaee مهدی ام حقیقی mahdi m. haghighi مینا اوحدی mina ohadi حسین نجم آبادی hossein najmabadi اصغر حاجی بیگی asghar hajibeigi

autosomal dominant polycystic kidney disease (adpkd) is the most common genetic nephropathy, which is characterized by replacement of renal parenchyma with multiple cysts. in iran, the disease prevalence within the chronic hemodialysis patient population is approximately 8-10%. so far, three genetic loci have been identified to be responsible for adpkd. little information is available concernin...

شهین دخت اشجعی, ,

Extract When a woman undergoes genetic testing of her fetus, the physiologic and emotional demands are great. Careful nursing assessment and support are vital. The main benefit of prenatal genetic diagnosis is that women be given the opportunity to coping with your pregnancy where fetal abnormalities has been diagnosed or achieve  to a complete relaxation with  the positive results obtained . E...

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