Invasive and Noninvasive Approaches in Prenatal Diagnosis of Thalassemias

Author:

Tuli Abdullah,Yenilmez Ebru Dündar

Publisher

InTech

Reference36 articles.

1. Nussbaum RL, McInnes RR, Willard HF. Thompson & Thompson Genetics in Medicine. Canada: Elsevier Health Sciences; 2015. p. 233

2. Tuzmen S, Schechter A. Genetic diseases of hemoglobin: Diagnostic methods for elucidating β-thalassemia mutations. Blood Reviews. 2001;15(1):19-29

3. Cappellini M-D, Cohen A, Porter J, Taher A, Viprakasit V. Guidelines for the management of transfusion dependent thalassaemia (TDT). TIF Publication. 2014;20:236

4. Cao A, Galanello R, Rosatelli MC. 8 prenatal diagnosis and screening of the haemoglobinopathies. Baillière's Clinical Haematology. 1998;11(1):215-238

5. Old J, Traeger-Synodinos J, Galanello R, Petrou M, Angastiniotis M. Prevention of thalassaemias and other haemoglobin disorders. Thalassaemia International Federation Publications. 2005;2:113-116

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