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Q27317126-93316D4C-DE2A-4952-9698-0015DEC87859
Q27317126-93316D4C-DE2A-4952-9698-0015DEC87859
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http://www.wikidata.org/entity/statement/Q27317126-93316D4C-DE2A-4952-9698-0015DEC87859
Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran
P2860
Q27317126-93316D4C-DE2A-4952-9698-0015DEC87859
BestRank
Statement
http://www.wikidata.org/entity/statement/Q27317126-93316D4C-DE2A-4952-9698-0015DEC87859
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02166044b6596a9deada29e04dbd1559f875e2a3
P2860
Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling.