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	1.	Hb Knossos (HBB: c.82G > T), β-globin CD 5 (-CT) (HBB: c.17_18delCT) and δ-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia. [electronic resource] by Moassas, Faten Nweder, Mohamad Sayah Murad, Hossam Producer: 20200304 In: BMC pediatrics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	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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