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	1.	PRF1 gene mutation in a Saudi patient with haemophagocytic lymphohistiocytosis. [electronic resource] by Al Balwi, M A Al Harbi, T Al Abdulkareem, I Hajeer, A H Producer: 20110606 In: British journal of biomedical science vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Congenital duplication of the palm syndrome: gene analysis and the molecular basis of its clinical features. [electronic resource] by Al-Qattan, M M Al-Balwi, M Eyaid, W Al-Abdulkarim, I Al-Turki, S Producer: 20090723 In: The Journal of hand surgery, European volume vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Detection of HCV antibody-negative donations: Saudi experience with nucleic acid testing. [electronic resource] by Hajeer, A H Al Gharawi, K Al Rayes, W Qasem, L Merenkov, Z Al Balwi, M Producer: 20090806 In: British journal of biomedical science vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	HLA-A, -B, -C, -DRB1 and -DQB1 allele and haplotype frequencies in Saudis using next generation sequencing technique. [electronic resource] by Hajeer, A H Al Balwi, M A Aytül Uyar, F Alhaidan, Y Alabdulrahman, A Al Abdulkareem, I Al Jumah, M Producer: 20140915 In: Tissue antigens vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Association of SNPs rs6498169 and rs10984447 with multiple sclerosis in Saudi patients: a model of the usefulness of familial aggregates in identifying genetic linkage in a multifactorial disease. [electronic resource] by Al Jumah, M Al Balwi, M Hussein, M Kojan, S Al Khathaami, A Al Fawaz, M Al Muzaini, B Jawhary, A Al Abdulkareem, I Producer: 20130419 In: Multiple sclerosis (Houndmills, Basingstoke, England) vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	The prevalence of CCR5-Δ32 mutation in a cohort of Saudi stem cell donors. [electronic resource] by Alarifi, M Al-Amro, F Alalwan, A Al-Turki, A Fakhoury, H Atallah, N Al-Muallimi, M Al-Balwi, M Alzahrani, M Alaskar, A Hajeer, A Jawdat, D Producer: 20180528 In: HLA vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	HLA class II polymorphism in Saudi patients with multiple sclerosis. [electronic resource] by Al Jumah, M Kojan, S Al Shehri, A M Al Balwi, M Al Abdulkarim, I Masuadi, E M Alhaidan, Y Alabdulrahman, A Fakhoury, H M Hajeer, A H Producer: 20190313 In: HLA vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomalies. [electronic resource] by Webb, Emma A AlMutair, Angham Kelberman, Daniel Bacchelli, Chiara Chanudet, Estelle Lescai, Francesco Andoniadou, Cynthia L Banyan, Abdul Alsawaid, Al Alrifai, Muhammad T Alahmesh, Mohammed A Balwi, M Mousavy-Gharavy, Seyedeh N Lukovic, Biljana Burke, Derek McCabe, Mark J Kasia, Tessa Kleta, Robert Stupka, Elia Beales, Philip L Thompson, Dorothy A Chong, W Kling Alkuraya, Fowzan S Martinez-Barbera, Juan-Pedro Sowden, Jane C Dattani, Mehul T Producer: 20131125 In: Brain : a journal of neurology vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)