Carmen Espinós

发表

Association of the 3467C>T mutation (T1156M) in the von Willebrand's factor gene with dominant type 1 von Willebrand's disease

F. Martínez, J. Aznar, S. Haya, 2001, Annals of Hematology.

Haemophilia B in a female caused by skewed inactivation of the normal X-chromosome.

F. Martínez, J. Aznar, J. I. Lorenzo, 2000, Haematologica.