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1
Q35068028-1E56E7A1-3D3D-4C2B-9FE0-480832B86B3A
Q35068028-1E56E7A1-3D3D-4C2B-9FE0-480832B86B3A
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http://www.wikidata.org/entity/statement/Q35068028-1E56E7A1-3D3D-4C2B-9FE0-480832B86B3A
Chromosome abnormalities and the genetics of congenital corneal opacification.
P2860
Q35068028-1E56E7A1-3D3D-4C2B-9FE0-480832B86B3A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35068028-1E56E7A1-3D3D-4C2B-9FE0-480832B86B3A
rank
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type
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Statement
wasDerivedFrom
1e4c0fe9f614d388801e127afb421c76542128d0
P2860
Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21)