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	1.	Connexin 26 gene mutations in non-syndromic hearing loss among Kuwaiti patients. [electronic resource] by Al-Sebeih, Khalid Al-Kandari, Marium Al-Awadi, Sadika A Hegazy, Fatma F Al-Khamees, Ghada A Naguib, Kamal K Al-Dabbous, Reem M Producer: 20140916 In: Medical principles and practice : international journal of the Kuwait University, Health Science Centre vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Using whole-exome sequencing to identify inherited causes of autism. [electronic resource] by Yu, Timothy W Chahrour, Maria H Coulter, Michael E Jiralerspong, Sarn Okamura-Ikeda, Kazuko Ataman, Bulent Schmitz-Abe, Klaus Harmin, David A Adli, Mazhar Malik, Athar N D'Gama, Alissa M Lim, Elaine T Sanders, Stephan J Mochida, Ganesh H Partlow, Jennifer N Sunu, Christine M Felie, Jillian M Rodriguez, Jacqueline Nasir, Ramzi H Ware, Janice Joseph, Robert M Hill, R Sean Kwan, Benjamin Y Al-Saffar, Muna Mukaddes, Nahit M Hashmi, Asif Balkhy, Soher Gascon, Generoso G Hisama, Fuki M LeClair, Elaine Poduri, Annapurna Oner, Ozgur Al-Saad, Samira Al-Awadi, Sadika A Bastaki, Laila Ben-Omran, Tawfeg Teebi, Ahmad S Al-Gazali, Lihadh Eapen, Valsamma Stevens, Christine R Rappaport, Leonard Gabriel, Stacey B Markianos, Kyriacos State, Matthew W Greenberg, Michael E Taniguchi, Hisaaki Braverman, Nancy E Morrow, Eric M Walsh, Christopher A Producer: 20130322 In: Neuron vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)