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Genetic variation at the NPT2 locus : implications for hereditary hypophosphatemic rickets with hypercalciuria and osteoporosis

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Identiferoai:union.ndltd.org:mcgill.ca/oai:escholarship.mcgill.ca:nz806172w
Date January 2000
CreatorsJones, Andrew Owain.
ContributorsTenenhouse, H. S. (Supervisor)
PublisherMcGill University
Source SetsMcGill University
Languagehttp://id.loc.gov/vocabulary/iso639-2/eng
Detected LanguageEnglish
TypeThesis
RightsAll items in eScholarship@McGill are protected by copyright with all rights reserved unless otherwise indicated.
RelationPid: 30843, Proquest: MQ70546

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