DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Padma G, Ramchander PV, Nandur UV, Padma T.
A rare event of maternal UPD in a proband with congenital non-syndromic hearing impairment with homozygosity for GJB2 p.W24X mutation.
Int J Genet Mol Biol 2010;
2 (06) 126-129
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