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pubmed-article:20083784pubmed:abstractTextTo document the audiologic phenotype of children with biallelic GJB2 (connexin 26) mutations, and to correlate it with the genotype.lld:pubmed
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pubmed-article:20083784pubmed:articleTitleAudiologic phenotype and progression in GJB2 (Connexin 26) hearing loss.lld:pubmed
pubmed-article:20083784pubmed:affiliationDepartment of Otolaryngology and Communication Enhancement, Children's Hospital Boston, 300 Longwood Ave, LO-367, Boston, MA 02115, USA. margaret.kenna@childrens.harvard.edulld:pubmed
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