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scopus(4)
Detection of beta thalassemia by the technique of refractory amplification of mutation systems (ARMS-PCR)
ArticleAbstract: beta Thalassemia (Thal) mutations were studied in DNA from 80/159 patients with hemolytic anemia andPalabras claves:Autores:Alvarez M., Arends A., Bravo M., Castillo O., Guevara J.M., Raquel Salazar-Lugo, Velázquez D.Fuentes:scopusDetermination of β-globin gene cluster haplotypes and prevalence of α- thalassemia in sickle cell anemia patients in Venezuela
ArticleAbstract: Sickle cell anemia and α-thalassemia have a heterogeneous distribution in Venezuela with a high freqPalabras claves:Sickle cell anemia, α-thalassemia, β-globin haplotypesAutores:Alvarez M., Arends A., Bravo M., Castillo O., Guevara J.M., Raquel Salazar-Lugo, Velázquez D.Fuentes:scopusHemoglobin alamo [α<inf>2</inf>β2l9(b1)asn → asp] in a venezuelan family
ArticleAbstract:Palabras claves:Autores:Anchustegui M., Arends T., Castillo O., Garlín G., Maleh Y., Raquel Salazar-LugoFuentes:scopusHemoglobin variants and hematologic and serologic parameters of the population of El Limón (Aragua State, Venezuela)
ArticleAbstract: Nine hundred and fifty seven individuals from El Limon (Aragua State, Venezuela) were studied, in orPalabras claves:Autores:Arends T., Castillo O., Leal M., Polanco W., Raquel Salazar-Lugo, Tapia T.Fuentes:scopus