References
- de Silva S, Fisher CA, Premawardhena A, Lamabadusuriya SP, Peto TEA, et al. 2000. Thalassaemia in Sri Lanka: implications for the future health burden of Asian populations. Lancet 355:786–791.
- Fisher CA, Premawardhena A, de Silva S, Perera G, Rajapaksa S, Olivieri NF, et al. 2003. The molecular basis for the thalassaemias in Sri Lanka. British Journal of Haematology 121:662–671.
- Joint SOGC-CCMG Clinical Practice Guideline. Oct 2008. Carrier Screening for Thalassemia and Hemoglobinopathies in Canada, No. 218.
- Kor-anantakul O, Suwanrath CT, Leetanaporn R, Suntharasaj T, Liabsuetrakul T, Rattanaprueksachart R. 1998. Prenatal diagnosis of thalassemia in Songklanagarind Hospital in southern Thailand. The Southeast Asian Journal of Tropical Medicine and Public Health 29:795–800.
- Monni G, Olla G, Rosatelli C, Cao A. 1990. Second-trimester placental biopsy versus amniocentesis for prenatal diagnosis of β-thalassemia. The New England Journal of Medicine 322:60–61.
- Ouali F, Siala H, Bibi A, Fradj SH, Dakhlaoui B, Othmani R, et al. 2015. Prenatal diagnosis of hemoglobinopathies: a case study in Tunisia. Journal of Blood Disorders & Transfusion 6:3.
- Phillips JA 3rd. 1980–1981. Prenatal diagnosis of sickle cell anemia and beta-thalassemia by amniocentesis. Texas Reports on Biology & Medicine 40:261–272.
- Premawardhena A, de Silva S, Arambepola M, Olivieri N, Merson L, Muraco J, et al. 2004. Thalassemia in Sri Lanka: a progress report. Human Molecular Genetics 13:R203–R206.
- Royal College of Obstetricians & Gynaecologists: Green-Top Guideline No. 8: June 2010, Update Dec 2014, Amniocentesis and Chorionic Villus sampling.
- SOGC Clinical Practice Guideline. July 2015. Prenatal Diagnosis Procedures and Techniques No. 326