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	1.	A novel mutation in PRDM5 in brittle cornea syndrome. [electronic resource] by Aldahmesh, M A Mohamed, J Y Alkuraya, F S Producer: 20120507 In: Clinical genetics vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Homozygous truncation of SIX6 causes complex microphthalmia in humans. [electronic resource] by Aldahmesh, M A Khan, A O Hijazi, H Alkuraya, F S Producer: 20140221 In: Clinical genetics vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mutations in ALDH1A3 cause microphthalmia. [electronic resource] by Aldahmesh, M A Khan, A O Hijazi, H Alkuraya, F S Producer: 20140221 In: Clinical genetics vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Neuronal ceroid lipofuscinosis caused by MFSD8 mutations: a common theme emerging. [electronic resource] by Aldahmesh, M A Al-Hassnan, Z N Aldosari, M Alkuraya, F S Producer: 20091207 In: Neurogenetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Clinical and molecular characterisation of Bardet-Biedl syndrome in consanguineous populations: the power of homozygosity mapping. [electronic resource] by Abu Safieh, L Aldahmesh, M A Shamseldin, H Hashem, M Shaheen, R Alkuraya, H Al Hazzaa, S A F Al-Rajhi, A Alkuraya, F S Producer: 20100728 In: Journal of medical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Mutations in known disease genes account for the majority of autosomal recessive retinal dystrophies. [electronic resource] by Patel, N Alkuraya, H Alzahrani, S S Nowailaty, S R Seidahmed, M Z Alhemidan, A Ben-Omran, T Ghazi, N G Al-Aqeel, A Al-Owain, M Alzaidan, H I Faqeih, E Kurdi, W Rahbeeni, Z Ibrahim, N Abdulwahab, F Hashem, M Shaheen, R Abouelhoda, M Monies, D Khan, A O Aldahmesh, M A Alkuraya, Fowzan S Producer: 20191114 In: Clinical genetics vol. 94 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Genetic investigation of 93 families with microphthalmia or posterior microphthalmos. [electronic resource] by Patel, N Khan, A O Alsahli, S Abdel-Salam, G Nowilaty, S R Mansour, A M Nabil, A Al-Owain, M Sogati, S Salih, M A Kamal, A M Alsharif, H Alsaif, H S Alzahrani, S S Abdulwahab, F Ibrahim, N Hashem, M Faquih, T Shah, Z A Abouelhoda, M Monies, D Dasouki, M Shaheen, R Wakil, S M Aldahmesh, M A Alkuraya, F S Producer: 20191203 In: Clinical genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)