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	1.	A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family. [electronic resource] by Wakil, Salma M Bohlega, Saeed Hagos, Samya Baz, Batoul Al Dossari, Haya Ramzan, Khushnooda Al-Hassnan, Zuhair N Producer: 20130611 In: European journal of medical genetics vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	New Insights into the Impact of Genome-Wide Copy Number Variations on Complex Congenital Heart Disease in Saudi Arabia. [electronic resource] by Dasouki, Majed J Wakil, Salma M Al-Harazi, Olfat Alkorashy, Maarab Muiya, Nzioka P Andres, Editha Hagos, Samya Aldusery, Haya Dzimiri, Nduna Colak, Dilek Producer: 20201019 In: Omics : a journal of integrative biology vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>T. [electronic resource] by Wakil, Salma M Ramzan, Khushnooda Abuthuraya, Rula Hagos, Samya Al-Dossari, Haya Al-Omar, Rana Murad, Hatem Chedrawi, Aziza Al-Hassnan, Zuhair N Finsterer, Josef Bohlega, Saeed Producer: 20140304 In: Gene vol. 536 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs. [electronic resource] by Wakil, Salma M Ram, Ramesh Muiya, Nzioka P Mehta, Munish Andres, Editha Mazhar, Nejat Baz, Batoul Hagos, Samya Alshahid, Maie Meyer, Brian F Morahan, Grant Dzimiri, Nduna Producer: 20161025 In: Atherosclerosis vol. 245 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A study of the role of GATA4 polymorphism in cardiovascular metabolic disorders. [electronic resource] by Muiya, Nzioka P Wakil, Salma M Tahir, Asma I Hagos, Samya Najai, Mohammed Gueco, Daisy Al-Tassan, Nada Andres, Editha Mazher, Nejat Meyer, Brian F Dzimiri, Nduna Producer: 20140624 In: Human genomics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Data on common variants associated with coronary artery disease/myocardial infarction in ethnic Arabs. [electronic resource] by Wakil, Salma M Ram, Ramesh Muiya, Nzioka P Mehta, Munish Andres, Editha Mazhar, Nejat Baz, Batoul Hagos, Samya Alshahid, Maie Meyer, Brian F Morahan, Grant Dzimiri, Nduna Publication details: Data in brief Jun 2016 In: Data in brief vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Exome Sequencing: Mutilating Sensory Neuropathy with Spastic Paraplegia due to a Mutation in FAM134B Gene. [electronic resource] by Wakil, Salma M Monies, Dorota Hagos, Samya Al-Ajlan, Fahad Finsterer, Josef Al Qahtani, Aisha Ramzan, Khushnooda Al Humaidy, Rawan Al-Muhaizea, Mohamed A Meyer, Brian Bohlega, Saeed A Publication details: Case reports in genetics 2018 In: Case reports in genetics vol. 2018 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Mutations in SMG9, Encoding an Essential Component of Nonsense-Mediated Decay Machinery, Cause a Multiple Congenital Anomaly Syndrome in Humans and Mice. [electronic resource] by Shaheen, Ranad Anazi, Shams Ben-Omran, Tawfeg Seidahmed, Mohammed Zain Caddle, L Brianna Palmer, Kristina Ali, Rehab Alshidi, Tarfa Hagos, Samya Goodwin, Leslie Hashem, Mais Wakil, Salma M Abouelhoda, Mohamed Colak, Dilek Murray, Stephen A Alkuraya, Fowzan S Producer: 20160829 In: American journal of human genetics vol. 98 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	The clinical utility of molecular karyotyping for neurocognitive phenotypes in a consanguineous population. [electronic resource] by Al-Qattan, Sarah M Wakil, Salma M Anazi, Shamsa Alazami, Anas M Patel, Nisha Shaheen, Ranad Shamseldin, Hanan E Hagos, Samya T AlDossari, Haya M Salih, Mustafa A El Khashab, Heba Y Kentab, Amal Y AlNasser, Mohammed N Bashiri, Fahad A Kaya, Namik Hashem, Mais O Alkuraya, Fowzan S Producer: 20160614 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Autozygome maps dispensable DNA and reveals potential selective bias against nullizygosity. [electronic resource] by Khalak, Hanif G Wakil, Salma M Imtiaz, Faiqa Ramzan, Khushnooda Baz, Batoul Almostafa, Abeer Hagos, Samya Alzahrani, Fatema Abu-Dhaim, Nada Abu Safieh, Leen Al-Jbali, Latifa Al-Hamed, Mohammed S Monies, Dorota Aldahmesh, Mohammed Al-Dosari, Mohammed S Kaya, Namik Shamseldin, Hanan Shaheen, Ranad Al-Rashed, May Hashem, Mais Al-Tassan, Nada Meyer, Brian Alazami, Anas M Alkuraya, Fowzan S Producer: 20120830 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)