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Q48275976-2E373BF6-7699-44C3-BEB1-0F1E2CCBEA67
Q48275976-2E373BF6-7699-44C3-BEB1-0F1E2CCBEA67
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Statement
http://www.wikidata.org/entity/statement/Q48275976-2E373BF6-7699-44C3-BEB1-0F1E2CCBEA67
Prevalence of Mutations in Deafness-Causing Genes in Cochlear Implanted Patients with Profound Nonsyndromic Sensorineural Hearing Loss in Shandong Province, China.
P2860
Q48275976-2E373BF6-7699-44C3-BEB1-0F1E2CCBEA67
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48275976-2E373BF6-7699-44C3-BEB1-0F1E2CCBEA67
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wasDerivedFrom
b88f6416d1404f88f48f3fb8d56d0c374f85214b
P2860
Evaluation of newborn screening bloodspot-based genetic testing as second tier screen for bedside newborn hearing screening.