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	1.	A novel mutation in a large family causes a unique phenotype of Mucolipidosis IV. [electronic resource] by AlBakheet, AlBandary Qari, Aliya Colak, Dilek Rasheed, Anas Kaya, Namik Al-Sayed, Moeenaldeen Producer: 20131018 In: Gene vol. 526 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Novel V97G ASAH1 mutation found in Farber disease patients: unique appearance of the disease with an intermediate severity, and marked early involvement of central and peripheral nervous system. [electronic resource] by Chedrawi, Aziza K Al-Hassnan, Zuhair N Al-Muhaizea, Muhammad Colak, Dilek Al-Younes, Banan Albakheet, Albandary Tulba, Sahar Kaya, Namik Producer: 20120820 In: Brain & development vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Array comparative genomic hybridization (aCGH) reveals the largest novel deletion in PCCA found in a Saudi family with propionic acidemia. [electronic resource] by Kaya, Namik Al-Owain, Mohammad Albakheet, Albandary Colak, Dilek Al-Odaib, Ali Imtiaz, Faiqa Coskun, Serdar Al-Sayed, Moeenaldeen Al-Hassnan, Zuhair Al-Zaidan, Hamad Meyer, Brian Ozand, Pinar Producer: 20090310 In: European journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Age-specific gene expression signatures for breast tumors and cross-species conserved potential cancer progression markers in young women. [electronic resource] by Colak, Dilek Nofal, Asmaa Albakheet, Albandary Nirmal, Maimoona Jeprel, Hatim Eldali, Abdelmoneim Al-Tweigeri, Taher Tulbah, Asma Ajarim, Dahish Malik, Osama Al Inan, Mehmet S Kaya, Namik Park, Ben H Bin Amer, Suad M Producer: 20131230 In: PloS one vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Genomic and transcriptomic analyses distinguish classic Rett and Rett-like syndrome and reveals shared altered pathways. [electronic resource] by Colak, Dilek Al-Dhalaan, Hesham Nester, Michael Albakheet, Albandary Al-Younes, Banan Al-Hassnan, Zohair Al-Dosari, Mohammad Chedrawi, Aziza Al-Owain, Muhammad Abudheim, Nada Al-Alwan, Laila Al-Odaib, Ali Ozand, Pinar Inan, Mehmet Sait Kaya, Namik Producer: 20110510 In: Genomics vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	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)
	7.	Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delay. [electronic resource] by Al-Sayed, Moeenaldeen D Al-Zaidan, Hamad Albakheet, Albandary Hakami, Hana Kenana, Rosan Al-Yafee, Yusra Al-Dosary, Mazhor Qari, Alya Al-Sheddi, Tarfa Al-Muheiza, Muhammed Al-Qubbaj, Wafa Lakmache, Yamina Al-Hindi, Hindi Ghaziuddin, Muhammad Colak, Dilek Kaya, Namik Producer: 20140219 In: American journal of human genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Identification of novel genomic imbalances in Saudi patients with congenital heart disease. [electronic resource] by Al-Hassnan, Zuhair N Albawardi, Waad Almutairi, Faten AlMass, Rawan AlBakheet, Albandary Mustafa, Osama M AlQuait, Laila Shinwari, Zarghuna M A Wakil, Salma Salih, Mustafa A Al-Fayyadh, Majid Hassan, Saeed M Aljoufan, Mansour Al-Nakhli, Osima Levy, Brynn AlMaarik, Balsam Al-Hakami, Hana A Alsagob, Maysoon Colak, Dilek Kaya, Namik Publication details: Molecular cytogenetics 2018 In: Molecular cytogenetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A novel X-linked disorder with developmental delay and autistic features. [electronic resource] by Kaya, Namik Colak, Dilek Albakheet, Albandary Al-Owain, Mohammad Abu-Dheim, Nada Al-Younes, Banan Al-Zahrani, Jawaher Mukaddes, Nahit M Dervent, Aysin Al-Dosari, Naji Al-Odaib, Ali Kayaalp, Inci V Al-Sayed, Moeenaladin Al-Hassnan, Zuhair Nester, Michael J Al-Dosari, Mohammad Al-Dhalaan, Hesham Chedrawi, Aziza Gunoz, Hulya Karakas, Bedri Sakati, Nadia Alkuraya, Fowzan S Gascon, Generaso G Ozand, Pinar T Producer: 20120606 In: Annals of neurology vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)