Delineating the autistic phenotype in children with neurofibromatosis type 1.

Autor: Chisholm, Anita K.1,2,3 (AUTHOR), Haebich, Kristina M.1,2 (AUTHOR), Pride, Natalie A.4 (AUTHOR), Walsh, Karin S.5 (AUTHOR), Lami, Francesca1,2 (AUTHOR), Ure, Alex1,6,7 (AUTHOR), Maloof, Tiba2,3 (AUTHOR), Brignell, Amanda1,6 (AUTHOR), Rouel, Melissa4 (AUTHOR), Granader, Yael5 (AUTHOR), Maier, Alice1,2 (AUTHOR), Barton, Belinda4,8,9 (AUTHOR), Darke, Hayley1 (AUTHOR), Dabscheck, Gabriel1,2,3 (AUTHOR), Anderson, Vicki A.1,2,3 (AUTHOR), Williams, Katrina1,2,6,7 (AUTHOR), North, Kathryn N.1,2 (AUTHOR), Payne, Jonathan M.1,2,3 (AUTHOR) jonathan.payne@mcri.edu.au
Zdroj: Molecular Autism. 1/4/2022, Vol. 13 Issue 1, p1-17. 17p.
Databáze: Academic Search Ultimate
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