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[Association of hemoglobinopathy and alpha thalassemia. Study of 45 patients].
Ataulfo González F, Blázquez C, Ropero P, Briceño O, Alaez C, Polo M, Benavente C, Mateo M, Peña A, Villegas A; Grupo de Eritropatología. Ataulfo González F, et al. Among authors: benavente c. Med Clin (Barc). 2005 May 21;124(19):726-9. doi: 10.1157/13075443. Med Clin (Barc). 2005. PMID: 15919031 Spanish.
Nondeletional α-Thalassemia: Two New Mutations on the α2 Gene.
Ropero P, Arbeteta J, Nieto JM, González FA, González B, Villegas A, Benavente C. Ropero P, et al. Among authors: benavente c. Hemoglobin. 2020 Jan;44(1):17-19. doi: 10.1080/03630269.2020.1721020. Epub 2020 Jan 31. Hemoglobin. 2020. PMID: 32000548
Why is the novel Hb Miguel Servet visualised by CE-HPLC newborn and not by the CE-HPLC β-thalassaemia programme?
Recasens V, Montañés Á, Rodríguez-Vigil C, González Y, Hernández de Abajo G, Nieto JM, González Fernández B, González-Fernández FA, Villegas A, Benavente C, Ropero P. Recasens V, et al. Among authors: benavente c. J Clin Pathol. 2021 Mar;74(3):198-201. doi: 10.1136/jclinpath-2020-206812. Epub 2020 Aug 12. J Clin Pathol. 2021. PMID: 32796052
83 results