-
Jansen, NA, Braden, RO, Srivastava, S, Otness, EF, Lesca, G, Rossi, M, Nizon, M, Bernier, RA, Quelin, C, van Haeringen, A, et al.
Clinical delineation of SETBP1 haploinsufficiency disorder.
European Journal of Human Genetics
29(8)
:
1198 -1205
2021
view publication
-
Morgan, C, Fetters, L, Adde, L, Badawi, N, Bancale, A, Boyd, RN, Chorna, O, Cioni, G, Damiano, DL, Darrah, J, et al.
Early Intervention for Children Aged 0 to 2 Years With or at High Risk of Cerebral Palsy.
JAMA Pediatrics
175(8)
:
846 -858
2021
view publication
-
Chenausky, KV, Brignell, A, Morgan, AT, Norton, AC, Tager-Flusberg, HB, Schlaug, G, Guenther, FH.
A Modeling-Guided Case Study of Disordered Speech in Minimally Verbal Children With Autism Spectrum Disorder..
American Journal of Speech-Language Pathology
30(3S)
:
1542 -1557
2021
view publication
-
Braden, RO, Boyce, JO, Stutterd, CA, Pope, K, Goel, H, Leventer, RJ, Scheffer, IE, Morgan, AT.
Speech, Language, and Oromotor Skills in Patients With Polymicrogyria..
Neurology
96(14)
:
e1898 -e1912
2021
view publication
-
Brignell, A, Gu, C, Holm, A, Carrigg, B, Sheppard, DA, Amor, DJ, Morgan, AT.
Speech and language phenotype in Phelan-McDermid (22q13.3) syndrome.
European Journal of Human Genetics
29(4)
:
564 -574
2021
view publication