Molecular diagnosis of hemoglobinopathies and thalassemia
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference15 articles.
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2. Antenatal diagnosis of sickle cell anaemia by direct analysis of the sickle mutation;Chang;Lancet,1981
3. alpha-Globin gene organisation in blacks precludes the severe form of alpha-thalassaemia;Dozy;Nature,1979
4. Prenatal diagnosis of hemoglobin disorders: present and future strategies;Harteveld;Clin Biochem,2009
5. In utero diagnosis of hemoglobinopathies. Technic for obtaining fetal blood;Hobbins;N Engl J Med,1974
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1. Seamless gene correction of β-thalassemia mutations in patient-specific iPSCs using CRISPR/Cas9 and piggyBac;Genome Research;2014-08-05
2. Preimplantation genetic diagnosis, an alternative to conventional prenatal diagnosis of the hemoglobinopathies;International Journal of Laboratory Hematology;2013-04-03
3. Incidence of β-thalassemia carrier on 1495 couples in preconceptional period;The Journal of Maternal-Fetal & Neonatal Medicine;2012-10-30
4. The evolution of prenatal diagnosis;Prenatal Diagnosis;2010-06-22
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