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	1.	First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss. [electronic resource] by Al-Achkar, Walid Al-Halabi, Bassel Ali, Bashar Moassass, Faten Producer: 20170321 In: International journal of pediatric otorhinolaryngology vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Mutations of the Connexin 26 gene in families with non-syndromic hearing loss. [electronic resource] by Al-Achkar, Walid Moassass, Faten Al-Halabi, Bassel Al-Ablog, Ayman Producer: 20110712 In: Molecular medicine reports vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Investigation of the mtDNA mutations in Syrian families with non-syndromic sensorineural hearing loss. [electronic resource] by Moassass, Faten Al-Halabi, Bassel Nweder, Mohamad Sayah Al-Achkar, Walid Producer: 20181114 In: International journal of pediatric otorhinolaryngology vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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