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Q24514987-B44F596D-6EE2-481D-9DB3-3D86DD079CAE
Q24514987-B44F596D-6EE2-481D-9DB3-3D86DD079CAE
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http://www.wikidata.org/entity/statement/Q24514987-B44F596D-6EE2-481D-9DB3-3D86DD079CAE
Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinism
P2860
Q24514987-B44F596D-6EE2-481D-9DB3-3D86DD079CAE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24514987-B44F596D-6EE2-481D-9DB3-3D86DD079CAE
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wasDerivedFrom
986afb467a355f4e556c71daa3a067b9984355b8
P2860
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules