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Carrier detection and prenatal diagnosis of hemophilia A: 5-years experience at a hemophilia center

✍ Scribed by Elisabetta Sacchi; Anna Maria Randi; Luigina Tagliavacca; Maurizio Sampietro; Paola Primignani; Pier Mannucio Mannucci


Book ID
110572843
Publisher
Springer
Year
1992
Tongue
English
Weight
455 KB
Volume
21
Category
Article
ISSN
0940-5437

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Methods and strategies are described for the prenatal diagnosis of three common congenital disorders--alpha and beta thalassemias and hemophilia A. It is important to study the frequency of restriction fragment length polymorphisms and types of molecular defects in specific ethnic groups, since they