Literature DB >> 9766808

Prothrombin gene 20210 G-A mutation in Turkish patients with thrombosis.

A Gürgey, G Hicsönmez, H Parlak, G Balta, A Celiker.   

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Year:  1998        PMID： 9766808     DOI： 10.1002/(sici)1096-8652(199810)59:2<179::aid-ajh16>3.0.co;2-4

Source DB:  PubMed          Journal:  Am J Hematol        ISSN： 0361-8609            Impact factor:   10.047


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  3 in total

Review 1.  Behçet's disease and thrombophilia.

Authors:  M Leiba; Y Sidi; H Gur; A Leiba; M Ehrenfeld
Journal:  Ann Rheum Dis       Date:  2001-12       Impact factor: 19.103

2.  Case series of thromboembolic complications in childhood nephrotic syndrome: Hacettepe experience.

Authors:  Betul Tavil; Fehime Kara; Rezan Topaloglu; Selin Aytac; Sule Unal; Baris Kuskonmaz; Mualla Cetin; Nesrin Besbas; Fatma Gumruk
Journal:  Clin Exp Nephrol       Date:  2014-07-04       Impact factor: 2.801

3.  May thrombosis be a cause of congenital extremity absence?

Authors:  Gurkan Genc; Nilgun Erkek Atay; Eda Kepenekli; Nese Yarali
Journal:  Indian J Pediatr       Date:  2007-05       Impact factor: 5.319
  3 in total

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