References
- Weatherall, D.J. and Clegg, J.B. (1996) "Thalassemia—a global public health problem", Nat. Med. 2, 847–849.
- Weatherall, D.J. (1998) "Thalassemia in the next millenuium. Keynote Address", Ann. NY Acad. Sci. 850, 1–9.
- Cao, A., Rosatelli, MC., Monni, G. and Galanello, R. (2002) "Screening for thalassemia: a model of success", Obstet. Gynecol. Clin. N. Am. 29, 305–328.
- Waye, J.S., Eng, B., Patterson, M., Walker, L., Carcao, M.D., Olivieri, N.F. and Chui, D.H. (2001) "Hemoglobin H (fib H) disease in Canada: molecular diagnosis and review of 116 cases", Am. J. Hematol. 68, 11–15.
- Rigoli, L., Meo, A., Miceli, MR., Alessio, K., Caruso, R.A., La Rosa, M.A., Salpietro, D.C., Ricca, M. and Barberi, I. (2001) "Molecular analysis of 13-thalassaemia patients in a high incidence area of southern Italy", Clin. Lab. Haematol. 23, 373–378.
- Villegas, A., Ropero, E, Gonzalez, EA., Anguita, E. and Espinos, D. (2001) "The thalassemia syndromes: molecular characterization in the Spanish population", Hemoglobin 25, 273–283.
- Chen, EE., Ooi, C., Ha, S.Y., Cheung, B.M.Y., Todd, D., Liang, R., Chan, T.K. and Chan, V. (2000) "Genetic and clinical features of hemoglobin H diseases in Chinese patients", N. Engl. J. Med. 343, 544–550.
- Zeng, Y.T., Huang, S.Z. and Chen, M.J. (1988) "The types of distribution of a-thalassemia-2 in China", Hemoglobin 12, 455–458.
- Yan, Z., Wu, G. and Wang, R. (1994) "Subtypes of non-deletion mutations in Chinese HbH patients", Chin. J. Hematol. 15, 393–395.
- Chu, D.C., Lee, C.H., Lo, M.D., Cheng, S.W., Chen, D.P., Wu, T.L., Tsao, K.C., Chiu, D.T. and Sun, C.F. (2000) "Non-radioactive Southern hybridization for early diagnosis of a-thalassemia with southeast Asian-type deletion in Taiwan", Am. J. Med. Gent. 95, 325–332.
- Liu, J., Zhu, J. and Wang, L. (2001) "Study on new techniques for genetic diagnosis of deletional a-thalassemia", Chin. J. Hematol. 22, 193–196.
- Saiki, R.K., Bugawan, T.L., Horn, G.T., Mullis, K.B. and Erlich, HA. (1986) "Analysis of enzymatically amplified 13 globin and HLA-DQ a DNA with allele-specific oligoneucleotide probes", Nature 324, 163–166.
- Olivieri, N.F. (1999) "The 13-thalassemias", N. Engl. J. Med. 341, 99–109.
- Wehtherall, D.J. (2001) "Phenotype-genotype relationships in monogenic disease: lessons from the thalassaemias", Nat. Rev. Genet. 2, 245–255.
- Globin Gene Disorder Working Party of the BCSH General Haematology Task Force (1994) "Guidelines for the fetal diagnosis of globin gene disorders", J. Clin. Pathol. 47, 199–204.
- Saiki, R.K., Walsh, P.S., Levenson, C.H. and Erlich, HA. (1989) "Genetic analysis of amplified DNA with immobilized sequence-specific oligonudeotide probes", Proc. Natl Acad. Sci. USA 86, 6230–6234.
- Tan, K.L., Tan, J.A., Wong, Y.C., Wee, Y.C., Thong, M.K. and Yap, S.F. (2001) "Combine-ARMS: a rapid and cost-effective protocol for molecular characterization of 13-thalassemia in Malaysia", Genet. Test 5, 17–22.
- Mao, Y.H., Sheng, M., Chen, M.J., Ren, Z.R. and Zeng, Y.T. (1996) "Prenatal diagnosis of 13 thalassemia using multiplex allele-specific amplification (MAS-PCR) in Chinese families", Hematology 1, 253–257.
- Piyamongkol, W., Harper, J.C., Delhanty, J.D. and Wells, D. (2001) "Preimplantation genetic diagnostic proto- cols for a- and 13-thalassaemias using multiplex fluorescent PCR", Prenatal Diagn. 21, 753–759.
- Weatherall, D.J. (2001) "The Thalassemia", In: Stamatoyan-nopoulos, G., Majerus, P.W., Perimutter, R.M. and Varmus, H., eds, The Molecular Basis of Blood Disease (Harcourt, Singapore), pp. 183–226.
- Gibbons, R.J. and Higgs, D.R. (2000) "Molecular-clinical spectrum of the ATR-X syndrome", Am. J. Med. Genet. 97, 204–212.
- Vrettou, C., Palmer, G., Kanavakis, E., Tzetis, M., Antoniadi, T., Mastrominas, M. and Traeger-Synodinos, J. (1999) "A widely applicable strategy for single cell genotyping of 13-thalassaemia mutations using DGGE analysis: application to preimplantation genetic diagnosis", Prenatal Diagn. 19, 1209–1216.
- Ganshirt, D., Smeets, F.W., Dohr, A., Walde, C., Steen, I., Lapucci, C., Falcinelli, C. and Sant, R. (1998) "Enrichment of fetal nucleated red blood cells from the maternal circulation for prenatal diagnosis: experiences with triple density gradient and MACS based on more than 600 cases", Fetal Diagn. Ther. 13, 276–286.
- Dubiley, S., Kirillov, E. and Mirzabekov, A. (1999) "Poly-morphism analysis and gene detection by minisequencing on an array of gel-immobilized primers", Nucleic Acids Res. 27, e19, (http://www.nar.oupjournal.org/cgi/content/full/27/18/e19).