Authors: Bin-Abbas, B Mawlawi, H Sakati, N Khafaja, Y Chaudhary, MA Al-Ashwal, A

Citation: B. Bin-abbas et al., Endocrine sequelae of childhood craniopharyngioma, J PED END M, 14(7), 2001, pp. 869-874

Authors: Iqbal, MA Sakati, N Nester, M Ozand, P

Citation: Ma. Iqbal et al., Cytogenetic diagnosis of fragile X syndrome: Study of 305 suspected cases in Saudi Arabia, ANN SAUDI M, 20(3-4), 2000, pp. 214-217

Authors: Diaz, GA Gelb, BD Ali, F Sakati, N Sanjad, S Meyer, BF Kambouris, M

Citation: Ga. Diaz et al., Sanjad-sakati and autosomal recessive Kenny-Caffey syndromes are allelic: Evidence for an ancestral founder mutation and locus refinement, AM J MED G, 85(1), 1999, pp. 48-52

Authors: Al-Jishi, E Meyer, BF Rashed, MS Al-Essa, M Al-Hamed, MH Sakati, N Sanjad, S Ozand, PT Kambouris, M

Citation: E. Al-jishi et al., Clinical, biochemical, and molecular characterization of patients with glutathione synthetase deficiency, CLIN GENET, 55(6), 1999, pp. 444-449

Authors: Wojcik, R Berg, MA Esposito, N Geffner, ME Sakati, N Reiter, EO Dower, S Francke, U Postel-Vinay, MC Finidori, J

Citation: R. Wojcik et al., Four contiguous amino acid substitutions, identified in patients with Laron syndrome, differently affect the binding affinity and intracellular trafficking of the growth hormone receptor, J CLIN END, 83(12), 1998, pp. 4481-4489