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	1.	Mutations in c12orf57 cause a syndromic form of colobomatous microphthalmia. [electronic resource] by Zahrani, Fatema Aldahmesh, Mohammed A Alshammari, Muneera J Al-Hazzaa, Selwa A F Alkuraya, Fowzan S Producer: 20130729 In: American journal of human genetics vol. 92 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	COL4A4-related nephropathy caused by a novel mutation in a large consanguineous Saudi family. [electronic resource] by Ramzan, Khushnooda Imtiaz, Faiqa Taibah, Khalid Alnufiee, Samir Akhtar, Mohammed Al-Hazzaa, Selwa A F Al-Owain, Mohammed Producer: 20141103 In: International journal of pediatric otorhinolaryngology vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Effect of Pegylated Interferon and Mitomycin C on Ocular Surface Squamous Neoplasia in Xeroderma Pigmentosum: A Case Series. [electronic resource] by Dirar, Qais S Musalem, Hebah M Al-Hazzaa, Selwa A F Al Zoba, Abdulaziz A Almalki, Amal A Producer: 20200924 In: The American journal of case reports vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Unusual Association of Aniridia with Aicardi-Goutières Syndrome-Related Congenital Glaucoma in a Tertiary Care Center. [electronic resource] by Musalem, Hebah M Dirar, Qais S Al-Hazzaa, Selwa A F Al Zoba, Abdul-Aziz A El-Mansoury, Jeylan Producer: 20181010 In: The American journal of case reports vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Utility of whole exome sequencing in the diagnosis of Usher syndrome: Report of novel compound heterozygous MYO7A mutations. [electronic resource] by Ramzan, Khushnooda Al-Owain, Mohammed Huma, Rozeena Al-Hazzaa, Selwa A F Al-Ageel, Sarah Imtiaz, Faiqa Al-Sayed, Moeenaldeen Producer: 20180710 In: International journal of pediatric otorhinolaryngology vol. 108 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	ILDR1: Novel mutation and a rare cause of congenital deafness in the Saudi Arabian population. [electronic resource] by Ramzan, Khushnooda Taibah, Khalid Tahir, Asma I Al-Tassan, Nada Berhan, Amal Khater, Ahmed M Al-Hazzaa, Selwa A F Al-Owain, Mohammed Imtiaz, Faiqa Producer: 20150206 In: European journal of medical genetics vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	RP1 and retinitis pigmentosa: report of novel mutations and insight into mutational mechanism. [electronic resource] by Al-Rashed, May Abu Safieh, Leen Alkuraya, Hisham Aldahmesh, Mohammed A Alzahrani, Jawaher Diya, Mohamed Hashem, Mais Hardcastle, Alison J Al-Hazzaa, Selwa A F Alkuraya, Fowzan S Producer: 20120906 In: The British journal of ophthalmology vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes. [electronic resource] by Abu-Safieh, Leen Alrashed, May Anazi, Shamsa Alkuraya, Hisham Khan, Arif O Al-Owain, Mohammed Al-Zahrani, Jawahir Al-Abdi, Lama Hashem, Mais Al-Tarimi, Salwa Sebai, Mohammed-Adeeb Shamia, Ahmed Ray-Zack, Mohamed D Nassan, Malik Al-Hassnan, Zuhair N Rahbeeni, Zuhair Waheeb, Saad Alkharashi, Abdullah Abboud, Emad Al-Hazzaa, Selwa A F Alkuraya, Fowzan S Producer: 20130715 In: Genome research vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies. [electronic resource] by Patel, Nisha Aldahmesh, Mohammed A Alkuraya, Hisham Anazi, Shamsa Alsharif, Hadeel Khan, Arif O Sunker, Asma Al-Mohsen, Saleh Abboud, Emad B Nowilaty, Sawsan R Alowain, Mohammed Al-Zaidan, Hamad Al-Saud, Bandar Alasmari, Ali Abdel-Salam, Ghada M H Abouelhoda, Mohamed Abdulwahab, Firdous M Ibrahim, Niema Naim, Ewa Al-Younes, Banan E AlMostafa, Abeer AlIssa, Abdulelah Hashem, Mais Buzovetsky, Olga Xiong, Yong Monies, Dorota Altassan, Nada Shaheen, Ranad Al-Hazzaa, Selwa A F Alkuraya, Fowzan S Producer: 20171211 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)