Prevalence of ACTN3 (the athlete gene) R577X polymorphism in Iranian population

por Fattahi, Z, Najmabadi, H
Publicado 2012

Investigation of Genetic Causes of Intellectual Disability in Kerman Province, South East of Iran

por Soltani Banavandi, M J, Kahrizi, K, Behjati, F, Mohseni, M, Darvish, H, Bahman, I, Abedinni, S S, Ghasemi Firouzabadi, S, Jafari, E, Ghadami, Sh, Sabbagh, F, Kavoosi, Gh R, Najmabadi, H
Publicado 2012

De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females

por Palmer, E E, Stuhlmann, T, Weinert, S, Haan, E, Van Esch, H, Holvoet, M, Boyle, J, Leffler, M, Raynaud, M, Moraine, C, van Bokhoven, H, Kleefstra, T, Kahrizi, K, Najmabadi, H, Ropers, H-H, Delgado, M R, Sirsi, D, Golla, S, Sommer, A, Pietryga, M P, Chung, W K, Wynn, J, Rohena, L, Bernardo, E, Hamlin, D, Faux, B M, Grange, D K, Manwaring, L, Tolmie, J, Joss, S, Cobben, J M, Duijkers, F A M, Goehringer, J M, Challman, T D, Hennig, F, Fischer, U, Grimme, A, Suckow, V, Musante, L, Nicholl, J, Shaw, M, Lodh, S P, Niu, Z, Rosenfeld, J A, Stankiewicz, P, Jentsch, T J, Gecz, J, Field, M, Kalscheuer, V M
Publicado 2018