Tài liệu tham khảo |
Loại |
Chi tiết |
3. Baig, S. M. (2007). Molecular diagnosis of β‐thalassemia by multiplex ARMS‐PCR: a cost effective method for developing countries like Pakistan.Prenatal diagnosis 27(6): 580-581 |
Sách, tạp chí |
Tiêu đề: |
Prenatal diagnosis |
Tác giả: |
Baig, S. M |
Năm: |
2007 |
|
6. Boonyawat, B., C. Monsereenusorn and C. Traivaree (2014). Molecular analysis of beta-globin gene mutations among Thai beta-thalassemia children: results from a single center study. The application of clinical genetics 7: 253 |
Sách, tạp chí |
Tiêu đề: |
The application of clinical genetics |
Tác giả: |
Boonyawat, B., C. Monsereenusorn and C. Traivaree |
Năm: |
2014 |
|
7. Borah, M. S., P. K. Bhattacharya, M. S. Pathak and D. Kalita (2016). A hospital based study of Hb variant and beta thalassaemia mutational pattern characterization among the people of Northeast region of India. Annals of Pathology and Laboratory Medicine 3(3): A134-140 |
Sách, tạp chí |
Tiêu đề: |
Annals of Pathology and Laboratory Medicine |
Tác giả: |
Borah, M. S., P. K. Bhattacharya, M. S. Pathak and D. Kalita |
Năm: |
2016 |
|
8. Cai, L., H. Bai, V. Mahairaki, Y. Gao, C. He, Y. Wen, Y. C. Jin, Y. Wang, R. L. Pan and A. Qasba (2018). A universal approach to correct various HBB gene mutations in human stem cells for gene therapy of beta‐thalassemia and sickle cell disease. Stem cells translational medicine 7(1):87-97 |
Sách, tạp chí |
Tiêu đề: |
Stem cells translational medicine |
Tác giả: |
Cai, L., H. Bai, V. Mahairaki, Y. Gao, C. He, Y. Wen, Y. C. Jin, Y. Wang, R. L. Pan and A. Qasba |
Năm: |
2018 |
|
11. Chang, J., P. Chen, S.-S. Chiou, L.-S. Lee, L.-I. Perng and T. Liu (1992). Rapid diagnosis of beta-thalassemia mutations in Chinese by naturally and amplified created restriction sites. Blood 80(8): 2092-2096 |
Sách, tạp chí |
Tiêu đề: |
Blood |
Tác giả: |
Chang, J., P. Chen, S.-S. Chiou, L.-S. Lee, L.-I. Perng and T. Liu |
Năm: |
1992 |
|
13. Colah, R., A. Gorakshakar and A. Nadkarni (2010). Global burden, distribution and prevention of β-thalassemias and hemoglobin E disorders.Expert review of hematology 3(1): 103-117 |
Sách, tạp chí |
Tiêu đề: |
Expert review of hematology |
Tác giả: |
Colah, R., A. Gorakshakar and A. Nadkarni |
Năm: |
2010 |
|
16. Cousens, N. E., C. L. Gaff, S. A. Metcalfe and M. B. Delatycki (2010). Carrier screening for beta-thalassaemia: a review of international practice.European Journal of Human Genetics 18(10): 1077-1083 |
Sách, tạp chí |
Tiêu đề: |
European Journal of Human Genetics |
Tác giả: |
Cousens, N. E., C. L. Gaff, S. A. Metcalfe and M. B. Delatycki |
Năm: |
2010 |
|
17. Craig, J., R. Barnetson, J. Prior, J. Raven and S. Thein (1994) Rapid detection of deletions causing delta beta thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification. Blood 83(6):1673-1682 |
Sách, tạp chí |
|
18. Cremonesi, L., M. Ferrari, P. C. Giordano, C. L. Harteveld, M. Kleanthous, T. Papasavva, G. P. Patrinos and J. Traeger-Synodinos (2007) An overview of current microarray-based human globin gene mutation detection methods.Hemoglobin 31(3): 289-311 |
Sách, tạp chí |
|
20. Dianzani, I., S. Forrest, C. Camaschella, E. Gottardi and R. Cotton (1991) Heterozygotes and homozygotes: discrimination by chemical cleavage of mismatch. American journal of human genetics 48(2): 423 |
Sách, tạp chí |
Tiêu đề: |
American journal of human genetics |
|
21. Faa, V., M. Rosatelli, R. Sardu, A. Meloni, C. Toffoli and A. Cao (1992) A simple electrophoretic procedure for fetal diagnosis of β‐thalassaemia due to short deletions. Prenatal diagnosis 12(11): 903-907 |
Sách, tạp chí |
Tiêu đề: |
Prenatal diagnosis |
|
22. Filon, D., A. Oppenheim, E. Rachmilewitz, R. Kot and D. B. Truc (2000) Molecular analysis of β-thalassemia in Vietnam. Hemoglobin 24(2): 99-104 |
Sách, tạp chí |
|
23. Flatz, G., T. Sanguansermsri, S. Sengchanh, D. Horst and J. Horst (2004) The ‘Hot Spot’of Hb E [β26 (B8) Glu→ Lys] in Southeast Asia: β‐Globin Anomalies in the Lao Theung Population of Southern Laos. Hemoglobin 28(3): 197-204 |
Sách, tạp chí |
|
24. Fucharoen, S. and P. Winichagoon (1987) Hemoglobinopathies in southeast Asia. Hemoglobin 11 (1): 65-88 |
Sách, tạp chí |
|
25. Fucharoen, S. and P. Winichagoon (2011) Haemoglobinopathies in southeast Asia. The Indian journal of medical research 134(4): 498 |
Sách, tạp chí |
Tiêu đề: |
The Indian journal of medical research |
|
26. Gabbianelli, M., O. Morsilli, A. Massa, L. Pasquini, P. Cianciulli, U. Testa and C. Peschle (2008) Effective erythropoiesis and HbF reactivation induced by kit ligand in β-thalassemia. Blood 111(1): 421-429 |
Sách, tạp chí |
|
27. Galanello, R., S. Barella, S. Satta, L. Maccioni, C. Pintor and A. Cao (2002). Homozygosity for nondeletion δ-β0 thalassemia resulting in a silent clinical phenotype. Blood 100(5): 1913-1914 |
Sách, tạp chí |
Tiêu đề: |
Blood |
Tác giả: |
Galanello, R., S. Barella, S. Satta, L. Maccioni, C. Pintor and A. Cao |
Năm: |
2002 |
|
28. Galanello, R., R. Ruggeri, E. Paglietti, M. Addis, M. Melis and A. Cao (1983) A family with segregating triplicated alpha globin loci and beta thalassemia. Blood 62(5): 1035-1040 |
Sách, tạp chí |
|
29. Giordano, P. C., M. Bakker-Verwij and C. L. Harteveld (2009) Frequency of α-globin gene triplications and their interaction with β-thalassemia mutations. Hemoglobin 33(2): 124-131 |
Sách, tạp chí |
|
31. Gorakshakar, A., A. Pawar, A. Nadkarni, C. Lu, D. Monhanty, R. Krishnamoorthy, C. Besmond and R. Colah (1999) Potential of denaturing gradient gel electrophoresis for scanning of beta-thalassemia mutations in India. American journal of hematology 61(2): 120-125 |
Sách, tạp chí |
Tiêu đề: |
American journal of hematology |
|