نتایج جستجو برای: chromosomal anomalies

تعداد نتایج: 91765  

Journal: :Ultrasound in Obstetrics and Gynecology 2000

Journal: :مجله پزشکی مولکولی 0
pooneh nikuei molecular medicine research center, hormozgan university of medical sciences, bandar abbas, iran mehrdad mohtarami fertility and infertility research center, hormozgan university of medical sciences, bandar abbas, iran mohsen azad student research committee, hormozgan university of medical sciences, bandar abbas, iran fatemeh mohseni molecular medicine research center, hormozgan university of medical sciences, bandar abbas, iran fouzieh hajizadeh medical genetic counseling center, social welfare organization, bandar abbas, iran

introduction: mental retardation, is one of the most common causes for referral to genetic counseling centers, and is one of the greatest challenges in health care services in the world. down syndrome is the most common chromosomal abnormalities in humans. methods: this study performed in medical genetic counseling center of welfare organization in south of iran with high consanguineous marriag...

2014
Yan Yang Hexi Wang Min Gao Shuangshan Xu Xiaofen Xu Xinyu Cao Ying Tao

The aim of this study was to investigate the contribution of chromosomal anomalies and the frequency of particular types of aberrations in general couples preparing for pregnancy and make recommendations for pregnancy on the basis of the medical literature. A total of 6,198 general couples were included in the present study. The karyotypes were generated from the peripheral blood lymphocyte cul...

Journal: :Donald School Journal of Ultrasound in Obstetrics and Gynecology 2011

Journal: :Donald School Journal of Ultrasound in Obstetrics and Gynecology 2010

Journal: :Ultrasound in Obstetrics and Gynecology 2000

2010
Mohsen Akhavan Sepahi Behrouz Baraty Fatemeh Khalifeh Shooshtary

BACKGROUND HDR syndrome (hypoparathyroidism, sensorineural deafness and renal disease) is an autosomal dominant condition, defined by the triad hypoparathyroidism, renal dysplasia and hearing loss. Hirschsprung (HSCR) disease is a variable congenital absence of ganglion cells of the enteric nervous system resulting in degrees of functional bowel obstruction. Rarer chromosomal anomalies are repo...

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