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Q37138653-FA71DA11-B972-4181-A0A6-4B830CC519C1
Q37138653-FA71DA11-B972-4181-A0A6-4B830CC519C1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37138653-FA71DA11-B972-4181-A0A6-4B830CC519C1
NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traits.
P2860
Q37138653-FA71DA11-B972-4181-A0A6-4B830CC519C1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37138653-FA71DA11-B972-4181-A0A6-4B830CC519C1
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Statement
wasDerivedFrom
c3b6916df01c8f1719bcb21624fd66b5d055e9bd
P2860
A recurrent 1.71 Mb genomic imbalance at 2q13 increases the risk of developmental delay and dysmorphism.