نتایج جستجو برای: consanguinity

تعداد نتایج: 1500  

Journal: :Proceedings of the National Academy of Sciences 2009

Journal: :Annals of human genetics 2003
A D J Overall M Ahmad M G Thomas R A Nichols

We analysed microsatellite genotypes sampled from the Pakistani and Indian communities in Nottingham, UK, to investigate the genetic consequences of substructuring mediated by traditional marriage customs. The application of a recently developed likelihood approach identified significant levels of population substructure within the Pakistani community as a whole, as well as within the finer div...

Journal: :Journal of medical genetics 1972
P S Rao S G Inbaraj G Jesudian

Journal: :Human heredity 2014
Lihadh Al-Gazali Hanan Hamamy

Incidence rates of congenital disorders among the 350 million inhabitants of Arab countries could be influenced via the people's demographic and cultural characteristics. Arabs usually marry at a young age and have large families. They share certain core cultural values and beliefs, with the family accepted as the central structure of society. Consanguineous marriage is favored and respected in...

Journal: :Saudi medical journal 2000
S A Khoury D F Massad

OBJECTIVES Consanguinity is a wide spread practice in Jordan. The objective of this study is to explore the health effects of consanguinity, in particular fertility, reproductive wastage, infant mortality and congenital malformations. METHODS A stratified 2 stage cluster sample of 1867 married couples, representative of all population groups and all geographic locations of Jordan were randoml...

2015
Ravindra Kumar Vandana Arya Sarita Agarwal

Mutation spectrum varies significantly in different parts and different ethnic groups of India. Social factors such as preference to marry within the community and among 1st degree relatives (consanguinity) play an important role in impeding the gene pool of the disease within the community and so in society by and large. The present paper discusses the role of consanguinity in profiling of bet...

Journal: :Saudi medical journal 2007
Hanan A Hamamy Amira T Masri Azmy M Al-Hadidy Kamel M Ajlouni

OBJECTIVE With 20-30% of all marriages occurring between first cousins, increasing attention in Jordan is now given to role of consanguinity in the occurrence of genetic diseases. The objective of this study is to define the specific categories of genetic disorders associated with consanguineous marriages. METHODS Etiological categories and consanguinity rates were studied among 623 families ...

Journal: :international journal of molecular and cellular medicine 0
sahar shekoohi department of medical genetics, school of medicine, mashhad university of medical sciences, mashhad, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) majid mojarrad department of medical genetics, school of medicine, mashhad university of medical sciences, mashhad, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) reza raoofian department of medical genetics, school of medicine, mashhad university of medical sciences, mashhad, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) shahab ahmadzadeh department of medical genetics, school of medicine, mashhad university of medical sciences, mashhad, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) salmah mirzaie department of medical genetics, school of medicine, mashhad university of medical sciences, mashhad, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences) mohammad hassanzadeh-nazarabadi department of medical genetics, school of medicine, mashhad university of medical sciences, mashhad, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences)

spontaneous abortion (sab) is the most common complication of early pregnancy. numerous risk factors are associated with an increased risk of pregnancy loss such as: blighted ovum. the aim of this study was to determine the frequency of balanced chromosomal translocations in couples with a history of recurrent spontaneous abortions and ultrasound diagnosed blighted ovum. sixty eight couples wit...

Journal: :nephro-urology monthly 0
yasser elsayed matter department of dialysis and transplantation, the urology-nephrology center, mansoura university, mansoura, egypt; department of dialysis and transplantation, the urology-nephrology center, mansoura university, mansoura, egypt. fax: +20-502263717 ayman m nagib department of dialysis and transplantation, the urology-nephrology center, mansoura university, mansoura, egypt omar e lotfy department of nephrology, zagazig university, zagazig, egypt ahmed maher alsayed department of nephrology, zagazig university, zagazig, egypt ahmed f donia department of dialysis and transplantation, the urology-nephrology center, mansoura university, mansoura, egypt ayman f refaie department of dialysis and transplantation, the urology-nephrology center, mansoura university, mansoura, egypt

patients and methods from march 1976 to december 2013, the number of patients that underwent living renal transplantation sharing at least one hla haplotype with their donors was 2,485. we divided these patients into two groups: (1) 2,075 kidney transplant recipients (1,554 or 74.9% male and 521 or 25.1% female) for whom the donors were living related, (2) 410 kidney transplant recipients (297 ...

2011
Waleed Hamad Al Bu Ali Magdy Hassan Balaha Mohammed Saleh Al Moghannum Ibrahim Hashim

BACKGROUND Birth defects and inborn errors of metabolism are related to variable poor perinatal and neonatal outcomes. Our aim was to explore the pattern and prevalence of birth defects and metabolic birth errors in Al-Ahsa Governorate in the Eastern Province of Saudi Arabia. METHODS This retrospective case control study was done from April 2006 to 2009. Children with any birth defect or meta...

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