Hemophilia|https://phgkb.cdc.gov/GAPPKB/phgHome.do|Hemophilia

https://phgkb.cdc.gov/GAPPKB/phgHome.do

From HuGE Literature Finder Database

This database contains published literature on genetic associations and other human genome epidemiology

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• Genotyping of Intron Inversions and Point Mutations in Exon 14 of the FVIII Gene in Iranian Azeri Turkish Families with Hemophilia A.  
  Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2016 Dec 32 (4): 475-480.
  Shekari Khaniani Mahmoud, Ebrahimi Abdollah, Daraei Setareh, Derakhshan Sima Mansoo
• Variation in baseline factor VIII concentration in a retrospective cohort of mild/moderate hemophilia A patients carrying identical F8 mutations.  
  Journal of thrombosis and haemostasis : JTH 2016 Dec .
  Loomans J I, van Velzen A S, Eckhardt C L, Peters M, Mäkipernaa A, Holmstrom M, Brons P P, Dors N, Haya S, Voorberg J, van der Bom J G, Fijnvandraat
• Study of six patients with complete F9 deletion characterized by cytogenetic microarray: role of the SOX3 gene in intellectual disability.  
  Journal of thrombosis and haemostasis : JTH 2016 Oct 14 (10): 1988-1993.
  Jourdy Y, Chatron N, Carage M-L, Fretigny M, Meunier S, Zawadzki C, Gay V, Negrier C, Sanlaville D, Vinciguerra
• The higher prevalence of missense mutations in hemophilia B compared to hemophilia A could be important in determining a milder clinical phenotype in patients with severe hemophilia B.  
  Haematologica 2016 Oct 101 (10): e429.
  Melchiorre Daniela, Linari Silvia, Castaman Giancar
• Evaluation of factor VIII polymorphic short tandem repeat markers in linkage analysis for carrier diagnosis of hemophilia A.  
  Biomedical reports 2016 Aug 5 (2): 228-232.
  Shrestha Sabina, Dong Sufang, Li Zuhua, Huang Zhuliang, Zheng Fa

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