دورية أكاديمية

A novel α0‐thalassemia deletion in a Brazilian child with Hb H disease: −−Mococa.

التفاصيل البيبلوغرافية
العنوان: A novel α0‐thalassemia deletion in a Brazilian child with Hb H disease: −−Mococa.
المؤلفون: Soler, A. M., Pedroso, G. A., Geraldo, A. P. M., Albuquerque, D. M., Costa, F. F., Santos, M. N. N., Knijnenburg, J., Harteveld, C. L., Sonati, M. F., da Luz, J. A.
المصدر: International Journal of Laboratory Hematology; Aug2024, Vol. 46 Issue 4, p747-750, 4p
مصطلحات موضوعية: HEMOGLOBINOPATHY genetics, HYPOCHROMIC anemia, HIGH performance liquid chromatography, ALPHA-Thalassemia, BLOOD collection, POLYMERASE chain reaction, HEMOGLOBINOPATHY, FAMILY history (Medicine), DNA, GENETIC carriers, GENES, BRAZILIANS, GENETIC polymorphisms, GENETIC mutation, BLOOD diseases, ELECTROPHORESIS, SEQUENCE analysis, RETICULOCYTES, GENOTYPES, PHENOTYPES
قاعدة البيانات: Complementary Index
الوصف
تدمد:17515521
DOI:10.1111/ijlh.14277