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The following term was not found in PubMed: Korgeh
Page 1
The frequency of GJB2 mutations and the Delta (GJB6-D13S1830) deletion as a cause of autosomal recessive non-syndromic deafness in the Kurdish population.
Clin Genet. 2004 Jun;65(6):506-8. doi: 10.1111/j.1399-0004.2004.00262.x.
Clin Genet. 2004.
PMID: 15151513
No abstract available.
Dual V-type resonators to enhance beam quality of Yb:YAG thin-disk lasers.
Kazemi S, Mahdieh MH, Aghaie M.
Kazemi S, et al.
Appl Opt. 2016 Apr 1;55(10):2559-64. doi: 10.1364/AO.55.002559.
Appl Opt. 2016.
PMID: 27139657
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