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

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.

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Main Author: Lee , Ling Sze
Format: Thesis
Language:English
Published: 2011
Subjects:
Online Access:http://eprints.usm.my/29700/1/Human_choromosome_4_sequencing_and_single_nucleotide_polymorphism.pdf
http://eprints.usm.my/29700/
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Institution: Universiti Sains Malaysia
Language: English
id my.usm.eprints.29700
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spelling my.usm.eprints.29700 http://eprints.usm.my/29700/ Human Chromosome 4 Sequencing And Stngle Nucleotide Polymorphism (SNP) Analysis Of An Achondroplasia Individual Lee , Ling Sze R5-920 Medicine (General) 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. 2011-02 Thesis NonPeerReviewed application/pdf en http://eprints.usm.my/29700/1/Human_choromosome_4_sequencing_and_single_nucleotide_polymorphism.pdf Lee , Ling Sze (2011) Human Chromosome 4 Sequencing And Stngle Nucleotide Polymorphism (SNP) Analysis Of An Achondroplasia Individual. Masters thesis, USM.
institution Universiti Sains Malaysia
building Hamzah Sendut Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Sains Malaysia
content_source USM Institutional Repository
url_provider http://eprints.usm.my/
language English
topic R5-920 Medicine (General)
spellingShingle R5-920 Medicine (General)
Lee , Ling Sze
Human Chromosome 4 Sequencing And Stngle Nucleotide Polymorphism (SNP) Analysis Of An Achondroplasia Individual
description 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.
format Thesis
author Lee , Ling Sze
author_facet Lee , Ling Sze
author_sort Lee , Ling Sze
title Human Chromosome 4 Sequencing And Stngle Nucleotide Polymorphism (SNP) Analysis Of An Achondroplasia Individual
title_short Human Chromosome 4 Sequencing And Stngle Nucleotide Polymorphism (SNP) Analysis Of An Achondroplasia Individual
title_full Human Chromosome 4 Sequencing And Stngle Nucleotide Polymorphism (SNP) Analysis Of An Achondroplasia Individual
title_fullStr Human Chromosome 4 Sequencing And Stngle Nucleotide Polymorphism (SNP) Analysis Of An Achondroplasia Individual
title_full_unstemmed Human Chromosome 4 Sequencing And Stngle Nucleotide Polymorphism (SNP) Analysis Of An Achondroplasia Individual
title_sort human chromosome 4 sequencing and stngle nucleotide polymorphism (snp) analysis of an achondroplasia individual
publishDate 2011
url http://eprints.usm.my/29700/1/Human_choromosome_4_sequencing_and_single_nucleotide_polymorphism.pdf
http://eprints.usm.my/29700/
_version_ 1643706968500600832