Associated Papers
Genetic modifiers of long-term survival in sickle cell anemia.
Wonkam A et al.
Clinical and Translational Medicine, 2020
32898326 (PubMed )
Supplement: CTM2-10-e152-s001.pdf
Factor 11 single-nucleotide variants in women with heavy menstrual bleeding.
Wiewel-Verschueren S et al.
Journal of Obstetrics and Gynaecology : the Journal of the Institute of Obstetrics and Gynaecology, 2017
Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins.
Carmi S et al.
Nature Communications, 2014
25203624 (PubMed )
Supplement: ncomms5835-s5.xlsx › List_of_all_discovered_variants
Population-specific spectrum of the F11 mutations in Koreans: evidence for a founder effect.
Kim J et al.
Clinical Genetics, 2012
Simultaneous genotyping of coagulation factor XI type II and type III mutations by multiplex real-time polymerase chain reaction to determine their prevalence in healthy and factor XI-deficient Italians.
Zadra G et al.
Haematologica, 2008
Molecular genetic analysis of severe coagulation factor XI deficiency in six Italian patients.
Zadra G et al.
Haematologica, 2004
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