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X-chromosome inactivation in female patients with Fabry disease.
Echevarria L, Benistan K, Toussaint A, Dubourg O, Hagege AA, Eladari D, Jabbour F, Beldjord C, De Mazancourt P, Germain DP. Echevarria L, et al. Among authors: jabbour f. Clin Genet. 2016 Jan;89(1):44-54. doi: 10.1111/cge.12613. Epub 2015 Jun 22. Clin Genet. 2016. PMID: 25974833
[Enzyme replacement therapy of lysosomal storage diseases].
Germain DP, Boucly C, Carlier RY, Caudron E, Charlier P, Colas F, Jabbour F, Martinez V, Mokhtari S, Orlikowski D, Pellegrini N, Perronne C, Prigent H, Rubinsztajn R, Benistan K. Germain DP, et al. Among authors: jabbour f. Rev Med Interne. 2010 Dec;31 Suppl 2:S279-91. doi: 10.1016/S0248-8663(10)70028-X. Rev Med Interne. 2010. PMID: 21211680 French.
A cornucopia of diversity-Ranunculales as a model lineage.
RanOmics group; Becker A, Bachelier JB, Carrive L, Conde E Silva N, Damerval C, Del Rio C, Deveaux Y, Di Stilio VS, Gong Y, Jabbour F, Kramer EM, Nadot S, Pabón-Mora N, Wang W. RanOmics group, et al. Among authors: jabbour f. J Exp Bot. 2024 Mar 27;75(7):1800-1822. doi: 10.1093/jxb/erad492. J Exp Bot. 2024. PMID: 38109712 Free PMC article. Review.
63 results