Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Steiger, Christine"'
Autor:
Kolesnik, Anna May, Jones, Emily Jane Harrison, Garg, Shruti, Green, Jonathan, Charman, Tony, Johnson, Mark Henry, Baron-Cohen, Simon, Begum-Ali, Jannath, Bolton, Patrick, Cheung, Celeste, Dafner, Leila, Davies, Kim, Elsabbagh, Mayada, Fernandes, Janice, Fish, Laurel, Gammer, Isobel, Greensmith, Marian, Gliga, Teodora, Kalwarowsky, Sarah, Liew, Michelle, Pasco, Greg, Pickles, Andrew, Ribeiro, Helena, Salomone, Erica, Taylor, Chloe, Tucker, Leslie, Wass, Sam, Burkitt-Wright, Emma, Evans, D. Gareth, Vassallo, Grace, Eelloo, Judith, West, Siobhan, Howard, Elizabeth, Hupton, Eileen, Huson, Sue, Lewis, Lauren, Tricker, Karen, Dobbie, Angus, Drimer, Ruth, Sharif, Saghira Malik, Baralle, Diane, Redman, Carolyn, Sharif, Saba, Symth, Carolyn, Lam, Wayne, Bradbury, Alyson, Harrower, Neil, Quarrell, Oliver, Bethell, Helen, Jones, Rachel, Musson, Susan, Prem, Catherine, Splitt, Miranda, Horridge, Karen, Steiger, Christine, Jim, Carly
Publikováno v:
Molecular Autism, Vol 8, Iss 1, Pp 1-13 (2017)
Molecular Autism
Kolesnik, A M, Jones, E J H, Garg, S, Green, J, Charman, T, Johnson, M 2017, ' Early development of infants with Neurofibromatosis Type 1 : A case series ', Molecular Autism, vol. 8, no. 62 . https://doi.org/10.1186/s13229-017-0178-0
Kolesnik, A M, Jones, E J H, Garg, S, Green, J, Charman, T, Johnson, M H, Baron-Cohen, S, Begum-Ali, J, Bolton, P, Cheung, C, Dafner, L, Davies, K, Elsabbagh, M, Fernandes, J, Fish, L, Gammer, I, Greensmith, M, Gliga, T, Kalwarowsky, S, Liew, M, Pasco, G, Pickles, A, Ribeiro, H, Salomone, E, Taylor, C, Tucker, L, Wass, S, Burkitt-Wright, E, Evans, D G, Vassallo, G, Eelloo, J, West, S, Howard, E, Hupton, E, Huson, S, Lewis, L, Tricker, K, Dobbie, A, Drimer, R, Sharif, S M, Baralle, D, Redman, C, Sharif, S, Symth, C, Lam, W, Bradbury, A, Harrower, N, Quarrell, O, Bethell, H, Jones, R & Eden-Basis Team 2017, ' Early development of infants with neurofibromatosis type 1 : a case series ', Molecular Autism, vol. 8, no. 1, 62 . https://doi.org/10.1186/s13229-017-0178-0
Molecular Autism
Kolesnik, A M, Jones, E J H, Garg, S, Green, J, Charman, T, Johnson, M 2017, ' Early development of infants with Neurofibromatosis Type 1 : A case series ', Molecular Autism, vol. 8, no. 62 . https://doi.org/10.1186/s13229-017-0178-0
Kolesnik, A M, Jones, E J H, Garg, S, Green, J, Charman, T, Johnson, M H, Baron-Cohen, S, Begum-Ali, J, Bolton, P, Cheung, C, Dafner, L, Davies, K, Elsabbagh, M, Fernandes, J, Fish, L, Gammer, I, Greensmith, M, Gliga, T, Kalwarowsky, S, Liew, M, Pasco, G, Pickles, A, Ribeiro, H, Salomone, E, Taylor, C, Tucker, L, Wass, S, Burkitt-Wright, E, Evans, D G, Vassallo, G, Eelloo, J, West, S, Howard, E, Hupton, E, Huson, S, Lewis, L, Tricker, K, Dobbie, A, Drimer, R, Sharif, S M, Baralle, D, Redman, C, Sharif, S, Symth, C, Lam, W, Bradbury, A, Harrower, N, Quarrell, O, Bethell, H, Jones, R & Eden-Basis Team 2017, ' Early development of infants with neurofibromatosis type 1 : a case series ', Molecular Autism, vol. 8, no. 1, 62 . https://doi.org/10.1186/s13229-017-0178-0
Background Prospective studies of infants at familial risk for autism spectrum disorder (ASD) have yielded insights into the earliest signs of the disorder but represent heterogeneous samples of unclear aetiology. Complementing this approach by study
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