Diagnosis of α+-Thalassemias by Determining the Ratio of the Two α-Globin Gene Copies by Oligonucleotide Hybridization and Melting Curve Analysis

Author:

Timmann Christian1,Moenkemeyer Florian1,Evans Jennifer A2,Foerster Birgit1,Tannich Egbert1,Haase Sylvia1,Sievertsen Juergen1,Kohne Elisabeth3,Horstmann Rolf D1

Affiliation:

1. Department of Molecular Medicine, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany, and Institute of Medical Biometry and Statistics, University Hospital Schleswig-Holstein—Campus Lübeck, Lübeck, Germany

2. Kumasi Centre for Collaborative Research, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana

3. Department of Paediatrics, University of Ulm, Ulm, Germany

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

Reference13 articles.

1. Higgs DR. Molecular mechanisms of α-thalassemia. Steinberg MH Forget BG Higgs DR Nagel RL eds. Disorders of hemoglobin: genetics, pathophysiology, and clinical Management2001:405-430 Cambridge University Press Cambridge, UK. .

2. Orkin SH. The duplicated human α globin genes lie close together in cellular DNA. Proc Natl Acad Sci U S A1978;75:5950-5954.

3. Old JM. Screening and genetic diagnosis of haemoglobin disorders. Blood Rev2003;17:43-53.

4. Weatherall DJ. Disorders of the synthesis or function of haemoglobin. Weatherall DJ Leddingham JGG Warell DA eds. Oxford textbook of medicine 2nd ed. 1987:19.108-19.130 Oxford University Press Oxford. .

5. Rigas DA, Kohler R D, Osgood EE. New hemoglobin possessing a higher electrophoretic mobility than normal adult hemoglobin. Science1955;121:372-375.

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