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Genetics of autoimmune thyroid disease in the Lebanese population.
Farra C, Awwad J, Fadlallah A, Sebaly G, Hage G, Souaid M, Ashkar H, Medlej R, Gannageh MH, Halaby G. Farra C, et al. Among authors: medlej r. J Community Genet. 2012 Oct;3(4):259-64. doi: 10.1007/s12687-012-0085-1. Epub 2012 Mar 6. J Community Genet. 2012. PMID: 22392440 Free PMC article.
Heterogeneity in clinical manifestation of autosomal dominant neurohypophyseal diabetes insipidus caused by a mutation encoding Ala-1-->Val in the signal peptide of the arginine vasopressin/neurophysin II/copeptin precursor.
Repaske DR, Medlej R, Gültekin EK, Krishnamani MR, Halaby G, Findling JW, Phillips JA 3rd. Repaske DR, et al. Among authors: medlej r. J Clin Endocrinol Metab. 1997 Jan;82(1):51-6. doi: 10.1210/jcem.82.1.3660. J Clin Endocrinol Metab. 1997. PMID: 8989232
[Virilizing tumor in a woman. Management].
Medlej R, Atallah N, Abboud J, Gédéon E, Halaby G. Medlej R, et al. J Med Liban. 1992;40(4):219-24. J Med Liban. 1992. PMID: 1339912 French.
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