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Transferrin (TF) polymorphism in Libyans.

作者信息

Sebetan I M

机构信息

Department of Laboratory Medicine and Pathology, Hamad General Hospital, Doha, Qatar.

出版信息

Int J Legal Med. 1993;106(1):51-2. doi: 10.1007/BF01225025.

Abstract

The genetic polymorphism of transferrin (TF) was investigated in 110 unrelated Libyans, using ultrathin layer polyacrylamide gel isoelectric focusing followed by staining with Coomassie brilliant blue R250. Five common and one rare phenotypes were observed. The estimated allele frequencies were as follow: TFC1 = 0.7455, TFC2 = 0.2091, TFC3 = 0.0409 and TFD = 0.0045. The theoretical exclusion rate in cases of disputed paternity is 19.2%.

摘要

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本文引用的文献

1
Human transferrin (Tf) and group-specific component (Gc) subtypes in Tunisia.
Hum Genet. 1981;59(1):60-3. doi: 10.1007/BF00278855.
4
Human transferrin polymorphism.
Hum Hered. 1987;37(2):65-81. doi: 10.1159/000153680.
5
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