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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.	A rare chronic myeloid leukemia case with Philadelphia chromosome, BCR-ABL e13a3 transcript and complex translocation involving four different chromosomes. [electronic resource] by Achkar, Walid Al Wafa, Abdulsamad Ali, Bashar Yousef Manvelyan, Marina Liehr, Thomas Publication details: Oncology letters Sep 2010 In: Oncology letters vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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