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Q37138653-29013455-8B33-49A7-9B4D-6DCE85E69E42
Q37138653-29013455-8B33-49A7-9B4D-6DCE85E69E42
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http://www.wikidata.org/entity/statement/Q37138653-29013455-8B33-49A7-9B4D-6DCE85E69E42
NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traits.
P2860
Q37138653-29013455-8B33-49A7-9B4D-6DCE85E69E42
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37138653-29013455-8B33-49A7-9B4D-6DCE85E69E42
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wasDerivedFrom
c3b6916df01c8f1719bcb21624fd66b5d055e9bd
P2860
A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes