Human chromosome 4 sequencing and single nucleotide polymorphism (SNP) analysis of an achondroplasia individual.

Achondroplasia adalah penyebab paling umum kekerdilan manusia 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.

Saved in:

Bibliographic Details
Main Author:	Lee, Ling Sze
Format:	Thesis
Language:	English
Published:	2011
Subjects:	QH1 Natural history (General - Including nature conservation, geographical distribution)
Online Access:	http://eprints.usm.my/41077/1/Human_chromosome_4_sequencing_and_single_nucleotide_polymorphism_%28SNP%29_analysis_of_an_achondroplasia_individual..pdf http://eprints.usm.my/41077/
Tags:	Add Tag No Tags, Be the first to tag this record!
Institution:	Universiti Sains Malaysia
Language:	English

id	my.usm.eprints.41077
record_format	eprints
spelling	my.usm.eprints.41077 http://eprints.usm.my/41077/ Human chromosome 4 sequencing and single nucleotide polymorphism (SNP) analysis of an achondroplasia individual. Lee, Ling Sze QH1 Natural history (General - Including nature conservation, geographical distribution) Achondroplasia adalah penyebab paling umum kekerdilan manusia 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/41077/1/Human_chromosome_4_sequencing_and_single_nucleotide_polymorphism_%28SNP%29_analysis_of_an_achondroplasia_individual..pdf Lee, Ling Sze (2011) Human chromosome 4 sequencing and single nucleotide polymorphism (SNP) analysis of an achondroplasia individual. Masters thesis, Universiti Sains Malaysia.
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	QH1 Natural history (General - Including nature conservation, geographical distribution)
spellingShingle	QH1 Natural history (General - Including nature conservation, geographical distribution) Lee, Ling Sze Human chromosome 4 sequencing and single nucleotide polymorphism (SNP) analysis of an achondroplasia individual.
description	Achondroplasia adalah penyebab paling umum kekerdilan manusia 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 single nucleotide polymorphism (SNP) analysis of an achondroplasia individual.
title_short	Human chromosome 4 sequencing and single nucleotide polymorphism (SNP) analysis of an achondroplasia individual.
title_full	Human chromosome 4 sequencing and single nucleotide polymorphism (SNP) analysis of an achondroplasia individual.
title_fullStr	Human chromosome 4 sequencing and single nucleotide polymorphism (SNP) analysis of an achondroplasia individual.
title_full_unstemmed	Human chromosome 4 sequencing and single nucleotide polymorphism (SNP) analysis of an achondroplasia individual.
title_sort	human chromosome 4 sequencing and single nucleotide polymorphism (snp) analysis of an achondroplasia individual.
publishDate	2011
url	http://eprints.usm.my/41077/1/Human_chromosome_4_sequencing_and_single_nucleotide_polymorphism_%28SNP%29_analysis_of_an_achondroplasia_individual..pdf http://eprints.usm.my/41077/
_version_	1643710122216652800

Human chromosome 4 sequencing and single nucleotide polymorphism (SNP) analysis of an achondroplasia individual.

Similar Items