Preconception carrier screening and prenatal diagnosis in thalassemia and hemoglobinopathies: challenges and future perspectives
Author:
Affiliation:
1. Department of Medical Genetics, National and Kapodistrian University of Athens, St. Sophia’s Children’s Hospital, Athens, Greece
2. Department of Clinical Genetics, Laboratory for Diagnostic Genome Analysis (LDGA), Leiden, The Netherlands
Publisher
Informa UK Limited
Subject
Genetics,Molecular Biology,Molecular Medicine,Pathology and Forensic Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/14737159.2017.1285701
Reference65 articles.
1. The Thalassaemia Syndromes
2. DOMINANT β THALASSAEMIA: MOLECULAR BASIS AND PATHOPHYSIOLOGY
3. First Report of a Dominantly Inherited β-Thalassemia Caused by a Novel Elongated β-Globin Chain
4. A KOREAN FAMILY WITH A DOMINANTLY INHERITED β-THALASSEMIA DUE TO Hb DURHAM-N.C./BRESCIA [β114(G16)Leu→Pro]
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