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Search Results - BandehiSarhaddi, Ameneh
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GJB2 c.−23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss
by
Zeinali, Sirous
,
Davoudi-Dehaghani, Elham
,
Azadmehr, Sarah
,
DabbaghBagheri, Samira
,
Bagherian, Hamideh
,
Jamali, Mojdeh
,
Zafarghandimotlagh, Fatemeh
,
Masoodifard, Mahboobeh
,
BandehiSarhaddi, Ameneh
,
Rejali, Leili
,
Sahebi, Sepideh
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European archives of oto-rhino-laryngology
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European Archives Of Oto-Rhino-Laryngology
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Arms-Pcr
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Autosomal Recessive Non-Syndromic Sensorineural Hearing Loss
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C.-23+1G>A
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C.−23+1G>A
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Connexin 26
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Connexins - Genetics
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Deafness
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Gene Frequency
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Gjb2
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Head And Neck Surgery
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Hearing Loss, Sensorineural - Genetics
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Humans
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Iran
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Ivs1+1G>A
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Medicine
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Medicine & Public Health
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Mutation
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Neurosurgery
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Otology
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Otorhinolaryngology
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Springer Nature
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