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: | Lee, Ling Sze |
---|---|
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!
|
Similar Items
-
Human Chromosome 4 Sequencing And
Single Nucleotide Polymorphism (Snp) Analysis
Of An Achondroplasia Individual
by: Lee , Ling Sze
Published: (2011) -
Human Chromosome 4 Sequencing And
Stngle Nucleotide Polymorphism (SNP) Analysis
Of An Achondroplasia Individual
by: Lee , Ling Sze
Published: (2011) -
Whole Genome Sequencing For Establishment Of Phylogenetic Position And Discovery Of Miniaturization And Lipid Metabolism Genes In Paedocypris
by: Sam, Ka Kei
Published: (2022) -
Effect of domestic effluent, agricultural and industrial pollution on aquatic macroinvertebrates with emphasis on chironomidae (diptera) at community, individual and molecular levels.
by: Al-Shami, Salman Abdo Ali
Published: (2011) -
Isolation, genome sequencing, assembly, annotation and Characterization of Thermus sp. CCB_US3_UF1 FROM Ulu Slim, Perak, Malaysia.
by: Teh, Beng Soon
Published: (2011)