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.
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Format: | Thesis |
Language: | English |
Published: |
2011
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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/ |
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