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:
Main Author: | |
---|---|
Format: | Thesis |
Language: | English |
Published: |
2011
|
Subjects: | |
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!
|
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 |
score |
13.211869 |