AAAAAA

   
Results: 1-8 |
Results: 8

Authors: Dawodu, A Dawson, KP Amirlak, I Kochiyil, J Agarwal, M Badrinath, P
Citation: A. Dawodu et al., Diet, clothing, sunshine exposure and micronutrient status of Arab infantsand young children, ANN TROP PA, 21(1), 2001, pp. 39-44

Authors: Al-Gazali, LI Padmanabhan, R Melnyk, S Yi, P Pogribny, IP Pogribna, M Bakir, M Hamid, ZA Abdulrazzaq, Y Dawodu, A James, SJ
Citation: Li. Al-gazali et al., Abnormal folate metabolism and genetic polymorphism of the folate pathway in a child with Down syndrome and neural tube defect, AM J MED G, 103(2), 2001, pp. 128-132

Authors: Al-Gazali, LI Bakir, M Dawodu, A Nath, R Al-Tatari, HM Gerami, M
Citation: Li. Al-gazali et al., Recurrence of the severe form of microgastria-limb reduction defect in a consanguineous family, CLIN DYSMOR, 8(4), 1999, pp. 253-258

Authors: Al-Gazali, LI Bakir, M Dawodu, A Haas, D
Citation: Li. Al-gazali et al., Recurrence of fibrochondrogenesis in a consanguineous family, CLIN DYSMOR, 8(1), 1999, pp. 59-61

Authors: Bayoumi, RA Dawodu, A Qureshi, MM Al-Khider, A Fitzgerald, P Riou, J Fisher, CA Fitches, A Old, JM
Citation: Ra. Bayoumi et al., The association of Hb Khartoum [beta 124(H2)Pro -> Arg] with gamma(+)-thalassemia is responsible for hemolytic disease in the newborn of a Sudanese family, HEMOGLOBIN, 23(1), 1999, pp. 33-45

Authors: Al-Gazali, LI Sztriha, L Dawodu, A Varady, E Bakir, M Khdir, A Johansen, J
Citation: Li. Al-gazali et al., Complex consanguinity associated with short rib-polydactyly syndrome III and congenital infection-like syndrome: a diagnostic problem in dysmorphic syndromes, J MED GENET, 36(6), 1999, pp. 461-466

Authors: Al-Gazali, L Sztriha, L Dawodu, A Bakir, M Varghese, M Varady, E Scorer, J Abdulrazzaq, Y Bener, A Padmanabhan, R
Citation: L. Al-gazali et al., Pattern of central nervous system anomalies in a population with a high rate of consanguineous marriages, CLIN GENET, 55(2), 1999, pp. 95-102

Authors: Abdulrazzaq, YM Micallef, R Qureshi, M Dawodu, A Ahmed, I Khidr, A Bastaki, SMA Al-Khayat, AI Bayoumi, RA
Citation: Ym. Abdulrazzaq et al., Diversity in expression of glucose-6-phosphate dehydrogenase deficiency infemales, CLIN GENET, 55(1), 1999, pp. 13-19
Risultati: 1-8 |