نتایج جستجو برای: genetic defect

تعداد نتایج: 700108  

Journal: :Genetical Research 1967

Journal: :journal of basic research in medical sciences 0
kourosh sayehmiri university of medical sciences ilam mohammad reza kaffashian department of physiology, faculty of medicine, ilam university of medical sciences, ilam, iran elahe ranaei department of anatomy, faculty of medicine, ilam university of medical sciences, ilam, iran

introduction: congenital anomalies are a common cause of disability and mortality in newborns and their treatments involves high costs for the society. this study aimed to investigate the prevalence of congenital anomalies and their causes. materials and methods: this research was a descriptive-analytical study and the population included all the newborns in hospitals of the city of ilam in 201...

Apert syndrome is a genetic defect which was first described by Eugene Apert in 1906. itchr('39')s incidence is approximately one in 50000 births. This syndrome is many abnormalities in your body and Central Nervous System. rehabilitation can increase children and their parentchr('39')s quality of life.We report a case of Apert syndrome and his occupational therapy program.

Journal: :Theriogenology 2005
Peter J Chenoweth

Genetic sperm defects are specific sperm defects, which have been shown to have a genetic mode of transmission. Such genetic linkage, either direct or indirect, has been associated with a number of sperm defects in different species, with this number increasing with improved diagnostic capabilities. A number of sperm defects, which have proven or suspected genetic modes of transmission are disc...

Journal: :genetics in the 3rd millennium 0
navid almadani farzaneh farhan fariba afroozan

larsen syndrome is a skeletal dysplasia (osteochondro-dysplasia) in which multiple dislocations of the large joints are the major feature . nosology in this group of disease, which constitutes 8% of mendelian disorders in man, is primarily based on clinical and radiological features. the underlying genetic defect is 3p21.1-p14.1 in the dominant type

Journal: :iranian rehabilitation journal 0
masoud gharib pediatric neurorehabilitation research center . university of social welfare and rehabilitation science,tehran,iran nazila akbar fahimi phd student of occupational therapy, occupational therapy department, university of social welfare and rehabilitation science,tehran,iran

apert syndrome is a genetic defect which was first described by eugene apert in 1906. it's incidence is approximately one in 50000 births. this syndrome is many abnormalities in your body and central nervous system. rehabilitation can increase children and their parent's quality of life.we report a case of apert syndrome and his occupational therapy program.

Journal: :Proceedings of the National Academy of Sciences 2010

Journal: :jentashapir journal of health research 0
maliheh abbasi leila m jouybari akram sanagoo samieh ghana

background diaphragm of eventration is a defect of whole or a part of diaphragm muscle and replacing it with fibroplastic tissue. the incidence of eventration is uncertain. the article aims to report a newborn with congenital diaphragmatic eventration. case report the case is a dysmorphic male premature newborn which born at 33 gestational age. due to sever respiratory distress the patient admi...

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