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Titlebook: Genetic Disorders of the Indian Subcontinent; Dhavendra Kumar Book 2004 Springer Science+Business Media New York 2004 Chromosom.developing

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书目名称Genetic Disorders of the Indian Subcontinent
编辑Dhavendra Kumar
视频video
概述The only book written and compiled on human genetics and genetic disorders affecting people of the Indian subcontinent.Provides a glossary for non-genetic professionals
图书封面Titlebook: Genetic Disorders of the Indian Subcontinent;  Dhavendra Kumar Book 2004 Springer Science+Business Media New York 2004 Chromosom.developing
描述The Indian subcontinent is a vast land mass inhabited by over one billion people. Its rich and varied history is reflected by its numerous racial and ethnic groups and its distinct religious, cultural and social characteristics. Like many developing countries in Asia, it is passing through both demographic and epidemiological transitions whereby, at least in some parts, the diseases of severe poverty are being replaced by those of Westemisation; obesity, diabetes, and heart disease, for example. Indeed, as we move into the new millennium India has become a land of opposites; on the one hand there is still extensive poverty yet, on the other hand, some of the most remarkable developments in commerce and technology in Asia are taking place, notably in the fields of information technology and biotechnology. India has always fascinated human geneticists and a considerable amount of work has been done towards tracing the origins of its different ethnic groups. In the current excitement generated by the human genome project and the molecular and genetic approach to the study of human disease, there is little doubt that this field will develop and flourish in India in the future. Although
出版日期Book 2004
关键词Chromosom; developing countries; development; genetics; infection; koffie; nutrition; pain; thrombosis
版次1
doihttps://doi.org/10.1007/978-1-4020-2231-9
isbn_softcover978-90-481-6262-8
isbn_ebook978-1-4020-2231-9
copyrightSpringer Science+Business Media New York 2004
The information of publication is updating

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Epidemiology of Genetic Diseasess is 67, 84, 17, and 51, respectively (State of the World’s Children, 2003). In all these countries there is an accelerating demographic switch to non-communicable diseases, particularly among the urban populations (Verma and Bijarnia, 2002). This is most apparent in Sri Lanka with its low mortality
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Immunogenetic Basis of Variation and Disease Susceptibilityble impact on developing new perspectives in molecular medicine. An understanding of the genetic basis of complex, multi-factorial diseases is crucial for identifying predisposing factors, assessing the effect of gene-environment interactions, predicting individual response to specific drugs and dis
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Consanguinity: Cultural, Religious and Social Aspects (Bittles, 1994). At a biological level, consanguineous unions may increase the risk in the homozygous state in their children [note 1] (Modell and Darr, 2003). This might be reflected in relatively higher probability of an autosomal recessive inherited disease and certain types of congenital malfor
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Congenital Developmental Anomaliesr about 3% of all children born in any hospital or in any country will have a significant congenital abnormality. It may be more than of cosmetic concern and which, if uncorrected, will interfere with normal functioning (Aase, 1990). Such anomalies occur in only a small fraction of all new born. How
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Malformation Syndromes in India multiple malformation syndromes associated with subtle dysmorphism and minor malformations may not become clinically relevant till later part of infancy or childhood when associated with developmental delay or mental retardation. Hence, incidence of multiple malformation syndromes obtained from exa
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Down Syndrome In Indiaenetics because, until then, human diploid constitution was believed to be 48. The impact of this discovery was soon felt in medical cytogenetics, when Lejeune et al (1959) reported that the common mental retardation disorder, Down syndrome [DS] was caused by trisomy of one of the G-group chromosome
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