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Tesis
Analisis Mutasi HBA2/HBA1 dan Polimorfisme Gen HBG2, BCL11A, HBS1L-MYB terhadap Tingkat Keparahan Klinis Pasien Thalassemia β
2026 | BY Ita Margaretha Nainggolan - Dwi Ari Pujianto - Annisa Octiandari Pertiwi- Analysis of HBA2/HBA1 Gene Mutation and HBG2, BCL11A, HBS1LMYB Polymorphisms with the Degree of Clinical Severity of b- Thalassemia patients.
- Nomor Panggil T26311fk
Disertasi
Mekanisme Molekuler Talasemia-α Berat yang Disebabkan Mutasi Kodon 59 (GGCGlisin→ GACAspartat) Gen Globin-2.
2014 | BY Ita Margaretha Nainggolan - Pustika Amalia Wahidiyat - Iswari Setianingsih - Alida R. Harahap- Molecular Mechanism of Severe -Thalassemia Due to Codon 59 Mutation GGCglycineGACaspartat 2-Globin Gene.
- Nomor Panggil D14017fk