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The Molecular Genetics of Hemophilia B

โœ Scribed by Valerie A. Geddes; Ross T.A. MacGillivray


Book ID
119552888
Publisher
Elsevier Science
Year
1987
Tongue
English
Weight
1005 KB
Volume
1
Category
Article
ISSN
1532-9496

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Prenatal and molecular diagnosis of hemo
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Prenatal diagnosis was carried out on a woman who had previously given birth to a son with a spontaneous mutation of C + T transition at nt 31133 of the factor IX (F.IX) gene. The diagnosis was performed on chorionic villi sampling by the method of amplificationcreated restriction site (ACRS). It re