Simple non-invasive prenatal detection of Hb Bart's disease by analysis of fetal erythrocytes in maternal blood
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference20 articles.
1. Prenatal Diagnosis of Homozygous αº-Thalassemia by an Immunological Method
2. Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum.
3. PCR Quantitation of Fetal Cells in Maternal Blood in Normal and Aneuploid Pregnancies**Presented in part at the annual meeting of the Society for Pediatric Research, Washington, DC, May 7, 1996, and at the 46th meeting of the American Society of Human Genetics, San Francisco, October 31, 1996.
4. Comparison of haemoglobin H inclusion bodies with embryonic zeta globin in screening for alpha thalassaemia.
5. Prenatal diagnosis of sickle cell anaemia and thalassaemia by analysis of fetal cells in maternal blood
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4. Hemoglobinopathies and Thalassemias;Emery and Rimoin's Principles and Practice of Medical Genetics;2013
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