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

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書目名稱Genetic Disorders of the Indian Subcontinent影響因子(影響力)




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Ingenuity

向下

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

lethal

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

甜瓜

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

甜瓜

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

Diluge

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

chlorosis

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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