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Beta-globin haplotypes from blood spots for follow-up of newborn hemoglobinopathy screening

✍ Scribed by Hiti, Alan L.; Zeng, Licheng; Xiang, Qing; Lorey, Fred W.; Powars, Darleen R.


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
47 KB
Volume
54
Category
Article
ISSN
0361-8609

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✦ Synopsis


The inheritance of sickle-cell anemia upon the background of the major ␤-globin gene cluster haplotypes has been associated with differing risks for major organ failure, and more recently with response to hydroxyurea treatment. Early identification of ␤-globin haplotypes in individuals with sickle-cell anemia may be a clinically useful prognostic factor for severity of disease expression. This report describes the use of whole-blood spots on filter papers from newborn hemoglobinopathy screening for ␤-globin gene cluster haplotyping by the polymerase chain reaction. Am.