Prenatal diagnosis of homozygous alpha thalassaemia by direct DNA analysis of uncultured amniotic fluid cells.

Author:

Chan V,Ghosh A,Chan T K,Wong V,Todd D

Publisher

BMJ

Subject

General Earth and Planetary Sciences,General Environmental Science,General Engineering

Reference18 articles.

1. The severe form of a thalassaemia is caused by a haemoglobin gene deletion;Ottolenghi, S.; Lanyon, W.G.; Paul, J.;Nature,1974

2. Genetic lesion in homozygous a thalassaemia (hydrops fetalis);Taylor, J.M.; Dozy, A.; Kan, Y.W.;Nature,1974

3. Gene deletions in a thalassemnia prove that the 5';Pressley, L.; Higgs, D.R.; Clegg, J.B.; Weatherall, D.J.,1980

4. Haemoglobin Barts hydrops syndrome in Greece. Br MedJ3;Kattamis, C.; Metaxotou-Mavromati, A.; Tsiarta, E.,1980

5. Embury SH, et al. a-Globin gene organisation in blacks precludes the severe form of a-thalassaemia;Dozy, A.M.; Kan, Y.W.;Nature,1979

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1. Comparison of Resistance Index and Peak Systolic Velocity of Fetal Middle Cerebral Artery between Normal and Fetuses with Mutated Beta-Thalassemia Gene;World Family Medicine Journal/Middle East Journal of Family Medicine;2018-01

2. Non-Immune Hydrops Fetalis;Asia-Oceania Journal of Obstetrics and Gynaecology;2010-05-24

3. Prenatal diagnosis of homozygous α0-thalassemia: from an invasive to a noninvasive approach;Expert Review of Obstetrics & Gynecology;2009-05

4. Alpha-thalassaemia;Seminars in Fetal and Neonatal Medicine;2008-08

5. Experience in preimplantation genetic diagnosis for exclusion of homozygous α° thalassemia;Prenatal Diagnosis;2006

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