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Q50346367-93281F99-B787-4017-9B6F-5609BE766682
Q50346367-93281F99-B787-4017-9B6F-5609BE766682
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http://www.wikidata.org/entity/statement/Q50346367-93281F99-B787-4017-9B6F-5609BE766682
A quantitative cSMART assay for noninvasive prenatal screening of autosomal recessive nonsyndromic hearing loss caused by GJB2 and SLC26A4 mutations.
P2860
Q50346367-93281F99-B787-4017-9B6F-5609BE766682
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50346367-93281F99-B787-4017-9B6F-5609BE766682
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wasDerivedFrom
3f14ec51baeeba453a3c0af954f7ed84cd1b11e4
P2860
Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents.