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	1.	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)
	2.	Down syndrome associated childhood myeloid leukemia with yet unreported acquired chromosomal abnormalities and a new potential adverse marker: dup(1)(q25q44). [electronic resource] by Moassass, Faten Wafa, Abdulsamad Liehr, Thomas Al-Ablog, Ayman Al Achkar, Walid Publication details: Molecular cytogenetics 2018 In: Molecular cytogenetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Acute promyelocytic leukemia with the translocation t(15;17)(q22;q21) associated with t(1;2)(q42~43;q11.2~12): a case report. [electronic resource] by Wafa, Abdulsamad Moassass, Faten Liehr, Thomas Al-Ablog, Ayman Al-Achkar, Walid Producer: 20170517 In: Journal of medical case reports vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Chromosomal aberration leads to recurrent pregnancy loss and partial trisomy of 5p12-15.3 in the offspring: report of a Syrian couple and review of the literature . [electronic resource] by Al-Achkar, Walid Moassass, Faten Al-Ablog, Ayman Liehr, Thomas Fan, Xiaobo Wafa, Abdulsamad Producer: 20150908 In: Zhonghua nan ke xue = National journal of andrology vol. 21 Availability: No items available. Save to lists Add to cart (remove)