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Publications by authors named "K Ali-Madadi"
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The frequency of GJB2 mutations and the Delta (GJB6-D13S1830) deletion as a cause of autosomal recessive non-syndromic deafness in the Kurdish population.
N Mahdieh
C Nishimura
K Ali-Madadi
Y Riazalhosseini
H Yazdan
Clin Genet
June 2004
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