Results 21 to 30 of about 52,020 (257)
Iranian Journal of Public Health, 1991 A total of 8641 married couples were investigated from 28 Iranian populations for consanguineous marriages and coefficient of inbreeding. The results showed considerable differences in the rate and kind of consanguineous matings among the various urban ...
D.D.Farhud +5 more
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Journal of Multidisciplinary Healthcare, 2023 Mustafa Ghanim,1 Rami Mosleh,2 Anas Hamdan,3 Johnny Amer,4 Malik Alqub,4 Yazun Jarrar,5 Majdi Dwikat4 1Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, An-Najah National University, Nablus, Palestine; 2Department of Pharmacy ...
Ghanim M +6 more
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The value question in India: Ethnographic reflections on an ongoing debate [PDF]
, 2020 The terms of the debate about anthropological approaches to the value question in India have been set by Dumont, whose theories were based on his ethnographic studies in North and South India, his knowledge of the Sanskrit literature, his synthesis of ...
Gregory, Chris
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Relationship of semen quality to inbreeding and gait of Colombian Creole horses
Ciência Rural, 2022 : High consanguinity among equines has negative effects on semen quality, thus resulting in low motility and high levels of abnormality in the spermatozoa.
Giovanni Restrepo Betancur +2 more
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The Economics of Consanguinity [PDF]
, 2006 The institution of consanguineous marriage - a marriage contracted between close biological relatives - has been a basic building block of many societies in different parts of the world.
Do, Quy-Toan +2 more
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Journal of Cleft Lip Palate and Craniofacial Anomalies, 2017 Context: Orofacial cleft (OFC) is one of the common craniofacial malformations. The etiology of these OFCs is multifactorial. One of the etiological factors is consanguinity (marriage between blood relatives).
B R Rajeev +3 more
doaj +1 more source
Biallelic mutations in valyl-tRNA synthetase gene VARS are associated with a progressive neurodevelopmental epileptic encephalopathy. [PDF]
, 2019 Aminoacyl-tRNA synthetases (ARSs) function to transfer amino acids to cognate tRNA molecules, which are required for protein translation. To date, biallelic mutations in 31 ARS genes are known to cause recessive, early-onset severe multi-organ diseases ...
Accogli, Andrea +28 more
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Progression of phenotype in Leber's congenital amaurosis with a mutation at the LCA5 locus [PDF]
, 2003 BACKGROUND: Leber’s congenital amaurosis (LCA) accounts for 5% of inherited retinal disease and is usually inherited as an autosomal recessive trait. Genetic and clinical heterogeneity exist.
Inglehearn, C.F. +5 more
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Studies on Maltese Consanguinity [PDF]
, 2003 The possible genetic consequences of consanguinity have been known from ancient times, though different societies have held varying views. Some have encouraged consanguinity as desirable and the classic examples are the sister brother marriages of the ...
Vassallo, Luis A.
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Role of fetal MRI in the evaluation of isolated and non-isolated corpus callosum dysgenesis: results of a cross-sectional study [PDF]
, 2017 PURPOSE: The aims of this study were to characterize isolated and non-isolated forms of corpus callosum dysgenesis (CCD) at fetal magnetic resonance imaging (MRI) and to identify early predictors of associated anomalies.
Antonelli, Amanda +11 more
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