1 |
Hemoglobin Disease Study Group. Survey of human hemoglobin of 600 000 cases in 20 provinces,cities,autonomous[J].Chin J Med, 1983,63:382-385.
|
2 |
Institute of Hematology, Chinese Academy of Medical Sciences, Hemoglobin Disease Study Group of 18 Provinces(Cities, Areas).Analysis of the abnormal hemoglobin in China[J].Chin J Med,1986,66:462-464.
|
3 |
Xu XM, Zhou YQ, Luo GX, et al. The prevalence and spectrum of αand β-Thelassemia in Guangdong province: Implications for the future health burden and population screening[J]. J Clin Pathol, 2004,57:517-522.
|
4 |
Li CG, Li CF, Li Q, et al. Thalassemia incidence and treatment in children with special reference to Shenzhen city and Guangdong province[J]. Hemoglobin, 2009,33:296-303.
|
5 |
Zhao ZM, Yao LQ, Fan LM, et al.Epidemilolgy investigation of Thalassemia of six national 0-7 years old children in Yunnan province environmental state on both sides[J].Chin J Epidemiolog,2011,32:352-356.
|
6 |
Ministry of Health of the People's Republic of China. Maternal and child health care and community health work in 2012[R].2012,6:1-3.
|
7 |
Fang JP, Xu LH. Criteria of diagnosis and treatment of Thalassemia[J].Chin J Pediatr,2010,48:166-169.
|
8 |
Huang SL, Fang JP, Zhou DH, et al.Treatment of severe β-Thalassemia by transplantation of umbilical cord blood hematopoietic stem cell[J].Chin J Pediatr,1998:671-674.
|
9 |
Zhu WG, Li XX, Yang M, et al. Treatment of severe β-Thalassemia by bone marrow trasplantation[J].Chin J Pediatr,2000:320-322.
|
10 |
Fang JP, Chen C, Huang SL, et al. Treatment of severe β-Thalassemia by allogeneic peripheral blood hematopoietic stem cell transplantation[J].Chin J Pediatr,2000:560-563.
|
11 |
Li C, Wu X, Feng X, et al. A novel conditioning regimen improves outcomes in β-thalassemia major patients using unrelated donor perioheral blood stem cell transplantation[J]. Blood, 2012,120:3875-3881.
|
12 |
WHO. Global applications of genomics in healthcare: Cyprus/Sardinia. Genomics and world health[R].Sumner Geneva Switzerland, WHO, 2002, 12,1-6.
|
13 |
Kalokairinou EM. The experience of beta-Thalassemin and its prevention in Cyprus[J]. Med Law, 2008,27:825-841.
|
14 |
Ministry of Health of the People's Republic of China. Maternal and child health care and community health work in 2012[R].2012, 9:1-6.
|
15 |
Zhou YQ, Li WD, Xu XM.The labolatory techniques for the screering of hereditary hemoglobinpathies[J]. Int J Genet,2008,31:17-22.
|
16 |
Urrechaga E. High-resolution HbA/C separation and hemoglobinpathy detection with capillary eletropheresis[J]. Am J Clin Pathol, 2012,138:448-456.
|
17 |
Urrechaga E, Borque L, Escanero JF. The role of automated measurement of red cell subpopulation on in differential diagnosis of microcytic anemia and β-Thalassemia screening[J]. Am J Clin Pathol,2011,135:374-379.
|
18 |
Bouva MJ, Sollaino C, Perseu L, et al. Relationship between neonatal screening results by HPLC and the number of α-Thalassemia gene mutation consequences for the cut-off value[J]. J Med Screen,2011,18:182-186.
|
19 |
Du CS. The present states and the future of the research of Thalassemia[J]. Chin J Genet,1996, 10:5-6
|
20 |
Cheung MC, Goldberg JD, Kan YW. Prenatal diagnosis of sickle cell anemia and Thalassemia by analysis of fetal cell in maternal blood[J]. Nat Genet 1996, 14:264-268.
|
21 |
Di Naro E, Ghezzi F, Vitucci A, et al. Prenatal diagnosis of beta-Thalassemia using fetal erythroblast enriched from maternal blood by novel gradient[J]. Mol Hum Reprod, 2000,6:571-574.
|
22 |
Xue JS, Long GF. Separation of the fetal nucleated erythrocyte from maternal blood and the noninvasive prenatal diagnosis[J]. Chin J Hematol,2000, 21: 512-516.
|
23 |
Wei HY, Long GF, Lin WX, et al. The application of the fetal mononucleated erythrocyte from maternal peripheral blood in the prenatal diagnosis of β-Thalassemia[J]. Chin J Pediatr, 2007,45:917-921
|
24 |
Lo YM, Corbetta N, Chamberlain PF, et al. Presence of fetal DNA in maternal plasma and serum[J]. Lancet, 1997, 350:485-487.
|
25 |
Lo YM, Chiu RW. Noninvasive approaches to prenatal diagnosis of hemoglobinopathies using fetal DNA in plasma[J]. Hemotol Oncol Clin North Am, 2010, 24: 1179-1186.
|
26 |
Lam KW, Jiang P, Liao GT, et al. Noninvasive prenatal diagnosis of monogenic diseases by targeted massively parallel sequencing of maternal plasma: Application to β-Thalassemia[J]. Clin Chem, 2012, 58:1467-1475.
|
27 |
Palmer GA, Traeger-Synodinos J, Davies S, et al. Pregnancies following blastocyst stage transfer in PGD cycles at risk for β-Thalassemic hemoglobinopathies[J]. Hum Reprod, 2002,17:25-31.
|