Últimas publicaciones
- Martorell-Sampol L, Tondo M, García-Fructuoso G, Naudo-Lahoz M, Alegre C, Gamez J, Genovés-Escarre J and Poo P Screening for the presence of FMR1 premutation alleles in a Spanish population with fibromyalgia CLINICAL RHEUMATOLOGY . 31(11): 1611-1615.
- Tondo M, Poo P, Naudo-Lahoz M, Ferrando T, Genovés-Escarre J, Molero M and Martorell-Sampol L Predisposition to epilepsy in fragile X syndrome: Does the Va166Met polymorphism in the BDNF gene play a role? EPILEPSY & BEHAVIOR . 22(3): 581-583.
- Martorell-Sampol L, Nascimento MT, Colomé-Roura R, Genovés-Escarre J, Naudo-Lahoz M and Nascimento-Osorio A Four sisters compound heterozygotes for the pre- and full mutation in fragile X syndrome and a complete inactivation of X-functional chromosome: implications for genetic counseling JOURNAL OF HUMAN GENETICS . 56(1): 87-90.