Human Chromosome 4 Sequencing And Stngle Nucleotide Polymorphism (SNP) Analysis Of An Achondroplasia Individual

Lee , Ling Sze (2011) Human Chromosome 4 Sequencing And Stngle Nucleotide Polymorphism (SNP) Analysis Of An Achondroplasia Individual. Masters thesis, USM.

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    Abstract

    Achondroplasia adalah penyebab paling umum kekerdilan manus1a yang beranggota pendek dan mempengaruhi seramai 250,000 orang di seluruh dunia. Achondroplasia is the most common cause of short-limbed dwarfism in humans, affecting 250,000 individuals worldwide.

    Item Type: Thesis (Masters)
    Subjects: R Medicine > R Medicine (General) > R5-920 Medicine (General)
    Divisions: Kampus Kesihatan (Health Campus) > Pusat Pengajian Sains Perubatan (School of Medical Sciences) > Thesis
    Depositing User: Mr Firdaus Mohamad
    Date Deposited: 17 Feb 2016 16:14
    Last Modified: 15 May 2017 12:43
    URI: http://eprints.usm.my/id/eprint/29700

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