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	1.	Mutations in CIT, encoding citron rho-interacting serine/threonine kinase, cause severe primary microcephaly in humans. [electronic resource] by Shaheen, Ranad Hashem, Amal Abdel-Salam, Ghada M H Al-Fadhli, Fatima Ewida, Nour Alkuraya, Fowzan S Producer: 20170519 In: Human genetics vol. 135 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	GZF1 Mutations Expand the Genetic Heterogeneity of Larsen Syndrome. [electronic resource] by Patel, Nisha Shamseldin, Hanan E Sakati, Nadia Khan, Arif O Softa, Ameen Al-Fadhli, Fatima M Hashem, Mais Abdulwahab, Firdous M Alshidi, Tarfa Alomar, Rana Alobeid, Eman Wakil, Salma M Colak, Dilek Alkuraya, Fowzan S Producer: 20170727 In: American journal of human genetics vol. 100 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Clinical and biochemical features associated with BCS1L mutation. [electronic resource] by Al-Owain, Mohammed Colak, Dilek Albakheet, Albandary Al-Younes, Banan Al-Humaidi, Zainab Al-Sayed, Moeen Al-Hindi, Hindi Al-Sugair, Abdulaziz Al-Muhaideb, Ahmed Rahbeeni, Zuhair Al-Sehli, Abdullah Al-Fadhli, Fatima Ozand, Pinar T Taylor, Robert W Kaya, Namik Producer: 20140519 In: Journal of inherited metabolic disease vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)