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1
Q41837986-DDE30CB8-5FF6-4421-A494-B02C40C3DB44
Q41837986-DDE30CB8-5FF6-4421-A494-B02C40C3DB44
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41837986-DDE30CB8-5FF6-4421-A494-B02C40C3DB44
A simple method to confirm and size deletion, duplication, and insertion mutations detected by sequence analysis.
P2860
Q41837986-DDE30CB8-5FF6-4421-A494-B02C40C3DB44
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41837986-DDE30CB8-5FF6-4421-A494-B02C40C3DB44
rank
NormalRank
type
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Statement
wasDerivedFrom
b0b95c938f8e2b8b42a55c0cae435af8a81fbb5f
P2860
Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss.