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Genetics of  Prader Willi Syndrome

 Table of contents:

Introduction:

Nature of Prader Willi Syndrome:

Etiology and Pathogenesis:

Genetics of Prader Willi Syndrome:

Animal Model:

Diagnostic Criteria:

Case Study:

Management:

Conclusion:

 

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With the completion of human genome sequencing, human genetics is poised for major developments in functional genomics, molecular diagnostics, pathogenesis of complex multifactorial diseases and gene-based therapy. This book includes manuscripts from an international symposium on human genetics and gene therapy as well as articles written by a selection of young researchers in the Asia Pacific region who are actively involved in a diverse range of medical problems, including cancers, infections, hypertension and myopia. New technologies being developed in gene therapy, lab-on-chips and bioinformatics are reported. The book provides a snapshot of the diverse approaches and solutions being developed at the frontiers of human genetics.


 

 

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