• English
    • Persian
    • English
    • Persian
  • English 
    • English
    • Persian
    • English
    • Persian
  • Login
Search 
  •   KR-TBZMED Home
  • Search
  •   KR-TBZMED Home
  • Search
JavaScript is disabled for your browser. Some features of this site may not work without it.

Search

Show Advanced FiltersHide Advanced Filters

Filters

Use filters to refine the search results.

Now showing items 1-1 of 1

  • Sort Options:
  • Relevance
  • Title Asc
  • Title Desc
  • Issue Date Asc
  • Issue Date Desc
  • Results Per Page:
  • 5
  • 10
  • 20
  • 40
  • 60
  • 80
  • 100
Thumbnail

Homozygosity for a Rare β0-Thalassemia Mutation [Frameshift Codons 25/26 (+T)] Causes β-Thalassemia Intermedia in an Iranian Family 

Haghi, M; Hosseinpour Feizi, AA; Harteveld, CL; Pouladi, N; Hosseinpour Feizi, MA (2009)
The severity of ?-thalassemia (?-thal) is remarkable for its variability in different populations, even in different patients. We studied a family from Azerbaijan Province, Northwestern Iran, who had a rare ?0-thal mutation, ...

Knowledge repository of Tabriz University of Medical Sciences using DSpace software copyright © 2018  HTMLMAP
Contact Us | Send Feedback
Theme by 
Atmire NV
 

 

Browse

All of KR-TBZMEDCommunities & CollectionsBy Issue DateAuthorsTitlesSubjects

My Account

LoginRegister

Discover

Author
Haghi, M (1)
Harteveld, CL (1)
Hosseinpour Feizi, AA (1)Hosseinpour Feizi, MA (1)Pouladi, N (1)Subjectadult (1)
article (1)
Azerbaijan (1)beta thalassemia (1)beta-Globins (1)beta-Thalassemia (1)Blood Transfusion (1)blood transfusion (1)child (1)clinical article (1)... View MoreDate Issued2009 (1)Has File(s)
No (1)

Knowledge repository of Tabriz University of Medical Sciences using DSpace software copyright © 2018  HTMLMAP
Contact Us | Send Feedback
Theme by 
Atmire NV