Experience in preimplantation genetic diagnosis for exclusion of homozygous α° thalassemia
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference28 articles.
1. A PCR-based strategy to detect the common severe determinants of α thalassaemia
2. Prenatal diagnosis of homozygous alpha thalassaemia by direct DNA analysis of uncultured amniotic fluid cells.
3. Organization of the ζ-α genes in Chinese
4. Diagnosis of spinal muscular atrophy from fetal normoblasts in maternal blood
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1. Hemoglobinopathies and Thalassemias;Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics;2023
2. Rapid Detection of Foetal Mendelian Disorders: Thalassaemia and Sickle Cell Syndrome;Prenatal Diagnostic Testing for Genetic Disorders;2023
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4. Prenatal Diagnosis of the Hemoglobinopathies;Genetic Disorders and the Fetus;2021-04-20
5. Knowledge, attitude and ethical consideration of Chinese couples requesting preimplantation genetic testing in Hong Kong;Journal of Obstetrics and Gynaecology Research;2019-02-11
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