Diagnosis Molekul Ovalositosis Dan Kaitannya Dengan Haplotipe Globin-B = Molecular Diagnosis Of Ovalocytosis And Its Relation With B-Globin Haplotypes
ABSTRACT Ovalocytosis is genetic trait commonly found in malaria endemic areas, hereditary in nature with oval-shaped red cells. The Molecular basis of SAO is a 27 by deletion in the gene of protein band-3 erythrocyte membrane. This genetic trait with one type of mutation, is widely found among the...
Main Author: | Perpustakaan UGM, i-lib |
---|---|
Format: | Article |
Published: |
[Yogyakarta] : Universitas Gadjah Mada
2002
|
Subjects: |
Similar Items
-
Diagnosis molekular ovalositosis dan kaitannya dengan haplptipe globin-Beta
by: , FUJIATI, et al.
Published: (2000) -
Detection of variant of hepatitis B virus and beta-globin through DNA technology
by: Chia, Chee Poh.
Published: (2009) -
Molecular characterisation of β-globin gene mutations in Penang and Kedah, Malaysia
by: Kho, Siew Leng, et al.
Published: (2014) -
Molecular defects in the beta-globin gene identified in different ethnic groups/populations during prenatal diagnosis for beta-thalassemia: a Malaysian experience
by: Tan, J., et al.
Published: (2004) -
Risk association, linkage disequilibrium, and haplotype analyses of ß-like globin gene polymorphisms with malaria risk in the Sabah population of Malaysian Borneo
by: Chong, Eric Tzyy Jiann, et al.
Published: (2022)