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Q33187450-9D1D752B-9775-42DC-ABF0-6F21278B8A39
Q33187450-9D1D752B-9775-42DC-ABF0-6F21278B8A39
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http://www.wikidata.org/entity/statement/Q33187450-9D1D752B-9775-42DC-ABF0-6F21278B8A39
Relation of PvuII site polymorphism in the COL1A2 gene to the risk of fractures in prepubertal Finnish girls.
P2860
Q33187450-9D1D752B-9775-42DC-ABF0-6F21278B8A39
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33187450-9D1D752B-9775-42DC-ABF0-6F21278B8A39
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wasDerivedFrom
9fa923ea99eeaaacb241a19342845007bc5a1cfb
P2860
An osteopenic nonfracture syndrome with features of mild osteogenesis imperfecta associated with the substitution of a cysteine for glycine at triple helix position 43 in the pro alpha 1(I) chain of type I collagen