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	1.	Two novel mutations of FBN1 in Jordanian patients with Marfan syndrome. [electronic resource] by Jaradat, Saied A Abujamous, Lama A Al-Hawamdeh, Ali A Alawneh, Khaldoon M Rawashdeh, Tamara A Jaradat, Zaher M Producer: 20160115 In: International journal of clinical and experimental medicine vol. 8 Availability: No items available. Save to lists Add to cart (remove)
	2.	Identification and Characterization of BTD Gene Mutations in Jordanian Children with Biotinidase Deficiency. [electronic resource] by Al-Eitan, Laith N Alqa'qa', Kifah Amayreh, Wajdi Khasawneh, Rame Aljamal, Hanan Al-Abed, Mamoon Haddad, Yazan Rawashdeh, Tamara Jaradat, Zaher Haddad, Hazem Publication details: Journal of personalized medicine Jan 2020 In: Journal of personalized medicine vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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