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

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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.

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/ http://eprints.usm.my/41077/1/Human_chromosome_4_sequencing_and_single_nucleotide_polymorphism_%28SNP%29_analysis_of_an_achondroplasia_individual..pdf

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