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	1.	Xq21.31-q21.32 duplication underlies intellectual disability in a large family with five affected males. [electronic resource] by Basit, Sulman Malibari, Omhani I Al-Balawi, Alia M Afzal, Sibtain Eldardear, Amr Elsayed Mohamed Ramzan, Khushnooda Producer: 20161013 In: American journal of medical genetics. Part A vol. 170A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder. [electronic resource] by Al-Hassnan, Zuhair N Al-Dosary, Mazhor Alfadhel, Majid Faqeih, Eissa A Alsagob, Maysoon Kenana, Rosan Almass, Rawan Al-Harazi, Olfat S Al-Hindi, Hindi Malibari, Omhani I Almutari, Faten B Tulbah, Sahar Alhadeq, Faten Al-Sheddi, Tarfa Alamro, Rana AlAsmari, Ali Almuntashri, Makki Alshaalan, Hesham Al-Mohanna, Futwan A Colak, Dilek Kaya, Namik Producer: 20160301 In: Journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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