Apert's syndrome: A rare case

Apert's syndrome is a rare type I acrocephalosyndactyly syndrome characterized by craniosynostosis, severe syndactyly of the hands and feet, and dysmorphic facial features. The purpose of this report is to present an Apert's syndrome patient by highlighting the craniofacial characteristics...

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Bibliographic Details
Main Authors: Tarun Kumar (Author), Neha Arora (Author), Gagan Puri (Author), Aravinda Konidena (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2016-01-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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