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	1.	Homozygous R396H mutation of the RAG1 gene in a Saudi infant with Omenn's syndrome: a case report. [electronic resource] by Al Balwi, Mohammed Al Ajaji, Sulaiman Al Abdulkareem, Ibrahim Hajeer, Ali Producer: 20110107 In: Cases journal vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A novel mutation in the SHH long-range regulator (ZRS) is associated with preaxial polydactyly, triphalangeal thumb, and severe radial ray deficiency. [electronic resource] by Al-Qattan, Mohammad M Al Abdulkareem, Ibrahim Al Haidan, Yazied Al Balwi, Mohammed Producer: 20130219 In: American journal of medical genetics. Part A vol. 158A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A novel homozygous missense mutation (c.610G>A, p.Gly204Ser) in the WNT7A gene causes tetra-amelia in two Saudi families. [electronic resource] by Eyaid, Wafaa Al-Qattan, Mohammad M Al Abdulkareem, Ibrahim Fetaini, Nouf Al Balwi, Mohammed Producer: 20110824 In: American journal of medical genetics. Part A vol. 155A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Clinical characteristics and genetic subtypes of Fanconi anemia in Saudi patients. [electronic resource] by Ghazwani, Yahya AlBalwi, Mohammed Al-Abdulkareem, Ibrahim Al-Dress, Mohammed Alharbi, Talal Alsudairy, Reem Alomari, Ali Aljamaan, Khalid Essa, Mohammed Al-Zahrani, Mohsen Alsultan, Abdulrahman Producer: 20160922 In: Cancer genetics vol. 209 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Monomeric C-reactive protein and Notch-3 co-operatively increase angiogenesis through PI3K signalling pathway. [electronic resource] by Boras, Emhamed Slevin, Mark Alexander, M Yvonne Aljohi, Ali Gilmore, William Ashworth, Jason Krupinski, Jerzy Potempa, Lawrence A Al Abdulkareem, Ibrahim Elobeid, Adila Matou-Nasri, Sabine Producer: 20150910 In: Cytokine vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Genome-wide association study of chronic hepatitis B virus infection reveals a novel candidate risk allele on 11q22.3. [electronic resource] by Al-Qahtani, Ahmed Khalak, Hanif G Alkuraya, Fowzan S Al-hamoudi, Waleed Al-hamoudy, Waleed Alswat, Khalid Al Balwi, Mohammed A Al Abdulkareem, Ibrahim Sanai, Faisal M Abdo, Ayman A Producer: 20140714 In: Journal of medical genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia. [electronic resource] by Tesson, Christelle Nawara, Magdalena Salih, Mustafa A M Rossignol, Rodrigue Zaki, Maha S Al Balwi, Mohammed Schule, Rebecca Mignot, Cyril Obre, Emilie Bouhouche, Ahmed Santorelli, Filippo M Durand, Christelle M Oteyza, Andrés Caballero El-Hachimi, Khalid H Al Drees, Abdulmajeed Bouslam, Naima Lamari, Foudil Elmalik, Salah A Kabiraj, Mohammad M Seidahmed, Mohammed Z Esteves, Typhaine Gaussen, Marion Monin, Marie-Lorraine Gyapay, Gabor Lechner, Doris Gonzalez, Michael Depienne, Christel Mochel, Fanny Lavie, Julie Schols, Ludger Lacombe, Didier Yahyaoui, Mohamed Al Abdulkareem, Ibrahim Zuchner, Stephan Yamashita, Atsushi Benomar, Ali Goizet, Cyril Durr, Alexandra Gleeson, Joseph G Darios, Frederic Brice, Alexis Stevanin, Giovanni Producer: 20130214 In: American journal of human genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)