Genetic counseling and genetic heterogeneity in the thalassemias
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1985.tb01209.x/fullpdf
Reference17 articles.
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2. Ceppellini , R. 1955 Biochemistry of Human Genetics. Ciba Foundation Symposium. G. E. Wolstenholme C. M. O'Connor 133
3. Two different molecular organizations account for the single α-globin gene of the α-thalassemia-2 genotype;Embury;J. Clin. Invest.,1980
4. Quantitation of Hb A2 with DE-52 microchromatography in whole blood as screening test for β-thalassemia heterozygotes;Galanello;Acta Haematol.,1977
5. DNA analysis in the diagnosis of hemoglobin disorders;Goossens;Methods Enzymol.,1981
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2. ICSH recommendations for the measurement of Haemoglobin A2;International Journal of Laboratory Hematology;2011-10-05
3. A 12-year preventive program for β-thalassemia in Northern Sardinia;Clinical Genetics;2008-06-28
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5. Control of β-thalassaemia by Carrier Screening, Genetic Counselling and Prenatal Diagnosis: The Sardinian Experience;Ciba Foundation Symposium 197 - Variation in the Human Genome;2007-09-28
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