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Low prevalence of DFNB1 (connexin 26) mutations in British Pakistani children with non-syndromic sensorineural hearing loss
Yoong,
S. Y..
Archives of Disease in Childhood.
v.
Vol.96.
no.
No.9.
2011-09.
p.
798 -
803...
issn:
0003-9888
.
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