1. Hercditary disorders of hacmostasis. In: Stanhury JB, Wyngaarden JB. Frederickson DS. 7'he metabolic basis of inlherited diseases;Ratnoff OD,1978
2. Characterisation of heterogcncity of haemophilia B for the detection of carriers;Panicucci, F.; Sagripante, A.; Pinori, Contc B.; E, Vispi; M, Lecchini; L.;Hae,1980
3. Isolation of a human antihaemophilic factor IX cDNA clonc using a unique 52-hase synthetic oligonucleotide probe deduced from the atmino acid scquence of hovine factor IX. Nucleic A cids Res;Jaye, M.; De La Salle, H.; Schamber, F.,1983
4. Molecular cloning of the gene for human anti-hacmophilic factor IX;Choo, K.H.; Gould, K.G.; Rees, D.J.G.; Brownlce, G.G.;Nature; human factor IX. Proc Natl Acad Sci; Isolation and charaictcrisation of cDNA coding for,1982
5. Regional localisation on the human X chromosome and polymorphism of the coagulation factor IX gene (haemophilia B locus);Camerino, G.; Jayc, Grzeschik K.H.; M.;Proc Natl Acad Sci USA