Cargando…
Prenatal Diagnosis of β-Thalassemias and Hemoglobinopathies.
Prenatal diagnosis of β-thalassemia was accomplished for the first time in the 1970s by globin chain synthesis analysis on fetal blood obtained by placental aspiration at 18–22 weeks gestation. Since then, the molecular definition of the β-globin gene pathology, the development of procedures of DNA...
Autores principales: | Rosatelli, Maria Cristina, Saba, Luisella |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Università Cattolica del Sacro Cuore
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3033155/ https://www.ncbi.nlm.nih.gov/pubmed/21415992 http://dx.doi.org/10.4084/MJHID.2009.011 |
Ejemplares similares
-
Gene Therapy in Thalassemia and Hemoglobinopathies
por: Breda, Laura, et al.
Publicado: (2009) -
Unexpected discovery of hemoglobinopathy C/β° thalassemia
por: Bouyarmane, Wafaa, et al.
Publicado: (2018) -
EHA Research Roadmap on Hemoglobinopathies and Thalassemia: An Update
por: Iolascon, Achille, et al.
Publicado: (2019) -
Infections in Thalassemia and Hemoglobinopathies: Focus on Therapy-Related Complications
por: Ricerca, Bianca Maria, et al.
Publicado: (2009) -
5612571 EARLIER PRENATAL DIAGNOSIS OF HEMOGLOBINOPATHIES BY CELOCENTESIS
por: Antonino Giambona, A.G., et al.
Publicado: (2023)