DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Pavithra A, Chandru J, Jeffrey JM, Karthikeyen NP, Srisailapathy CRS.
Rare compound heterozygosity involving dominant and recessive mutations of GJB2 gene in an assortative mating hearing impaired Indian family.
Eur Arch Otorhinolaryngol 2017;
274 (01) 119-125
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