6Old J,Traeger-Synodinos J,Galanello R,et al.Prevention of thalassaemias and other haemoglobin disorders.Vol 2.Nicosia,Cyprus:Thalassaemia International Federation,2005.1-39.
7Yong KN,Wadsworth D,Langlois S,et al.Thalassemia carrier screening and prenatal diagnosis among the British Columbia(Canada) population of Chinese descent.Clin Genet,1999,55:20-25.
8Liang R,Liang S,Jiang NH,et al.Alpha and beta thalassemia among Chinese children in Guangxi province,P.R.China:molecular and haematological chracterization.Br J Haematol,1994,86:351-354.
9Lam YH,Ghosh A,Tang MH,et al.The risk of alpha-thalassaemia in offspring of beta-thalassaemia carriers in Hong Kong,1997,17:733-736.
10Shiang R, Thompson L M, Zhu Y Z, et al. Fielder TJ, Bocian M, Winokur ST, Wasmuth JJ. Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia[J]. Cell, 1994,78(2): 335 -342.
4Cao A, Galanello R, RosateUi Mc. Prenatal diagnosis and screening of the haemoglobinopathies[ J ]. Baillieres Clin Haematol, 1998, 11 ( 1 ):215 - 238.
5Yong KN, Wadsworth D, Langlois S, et al. Thalassemia carrier screen- ing and prenatal diagnosis among the British Columbia(Canada) popula- tion of Chinese descent[ J]. Clin Genet, 1999, 55( 1 ) :20-25.
