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Hemoglobin
international journal for hemoglobin research
Volume 19, 1995 - Issue 5
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Original Article

Advances in the Prenatal and Molecular Diagnosis of the Hemoglobinopathies and Thalassemias

S. H. Embury The University of California San Francisco School of Medicine The Hematology Division, San Francisco General Hospital The Northern California Comprehensive Sickle Cell Center San Francisco, CA, 94110, USA
Pages 237-261 | Received 01 Feb 1995, Accepted 31 May 1995, Published online: 07 Jul 2009

Citations (13)

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N. S. Smetanina, T. P. Molchanova & T. H. J. Huisman. (1997) Analysis of Mrna from Red Cells of Patients with Thalassemia and Hemoglobin Variants. Hemoglobin 21:5, pages 437-467.
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Articles from other publishers (12)

Shahram Akhlaghpoor. (2006) Chorionic villus sampling for beta-thalassemia: the first report of experience in Iran. Prenatal Diagnosis 26:12, pages 1131-1136.
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Liane Esteves Daudt, Débora Zechmaister, Liliana Portal, Eurico Camargo Neto, Lúcia Mariano da Rocha Silla & Roberto Giugliani. (2002) Triagem neonatal para hemoglobinopatias: um estudo piloto em Porto Alegre, Rio Grande do Sul, Brasil. Cadernos de Saúde Pública 18:3, pages 833-841.
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S. Tuzmen & A.N. Schechter. (2001) Genetic diseases of hemoglobin: diagnostic methods for elucidating β -thalassemia mutations. Blood Reviews 15:1, pages 19-29.
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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
Chitra Thakur (Mahadik)Flavian Vaz, Monisha Banerjee, Chhaya Kapadia, P. G. Natrajan, Harsha Yagnik & Sudha Gangal. (2000) Prenatal diagnosis of ?-thalassaemia and other haemoglobinopathies in India. Prenatal Diagnosis 20:3, pages 194-201.
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Flora H. Fodor & Christine M. Eng. (1999) Molecular exclusion of haemoglobin SD disease by prenatal diagnosis. Prenatal Diagnosis 19:1, pages 58-60.
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Luis A. Ugozzoli, J. D. Lowery, A. A. Reyes, C.-I. P. Lin, A. Re, F. Locati, R. Galanello, L. Macioni, A. Maggio, A. Giambona, A. Loutradi, M. Boussiou & R. Bruce Wallace. (1998) Evaluation of the BeTha Gene 1 Kit for the Qualitative Detection of the Eight Most Common Mediterranean β-Thalassemia Mutations. American Journal of Hematology 59:3, pages 214-222.
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Tsang-Ming Ko, Li-Hui Tseng, Chuan-Hong Kao, Yu-Wan Lin, Hsiao-Lin Hwa, Pi-Mei Hsu, Shue-Fun Li & Sou-Ming Chuang. (1998) Molecular characterization and PCR diagnosis of Thailand deletion of α-globin gene cluster. American Journal of Hematology 57:2, pages 124-130.
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Néstor W. Soria, Clara L. Tulián, François Plassa & German A. Roth. (1997) β-thalassemia and hemoglobin types in Argentina: Determination of most frequent mutations. American Journal of Hematology 54:2, pages 160-163.
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John Old. (1996) Haemoglobinopathies. Prenatal Diagnosis 16:13, pages 1181-1186.
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M. Romana, L. Keclard, G. Guillemin, E. Lavocat, C. Saint‐Martin, C. Berchel & G. Mérault. (1998) Molecular characterization of β‐thalassemia mutations in Guadeloupe. American Journal of Hematology 53:4, pages 228-233.
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PRANEE SUTCHARITCHAN, RANDALL SAIKI, SUTHAT FUCHAROEN, PRANEE WINICHAGOON, HENRY ERLICH & STEPHEN H. EMBURY. (2008) Reverse dot‐blot detection of Thai β‐thalassaemia mutations. British Journal of Haematology 90:4, pages 809-816.
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