Craniosynostosis in 10q26 deletion patients: A consequence of brain underdevelopment or altered suture biology?

Autor: Flavia Imbroisi Valle Errera, Ágatha Cristhina Faria, Naila Cristina Vilaça Lourenço, Gerson Shigeru Kobayashi, Maria Regina Galvêas Oliveira Rebouças, Eliete Rabbi-Bortolini, Andreia L. A. de S. Thiago Pereira, Milena G. Tonini Frasson, Carla Rosenberg, Rodrigo Atique, Maria Rita Passos-Bueno

Publikováno v: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP

Approximately a hundred patients with terminal 10q deletions have been described. They present with a wide range of clinical features always accompanied by delayed development, intellectual disability and craniofacial dysmorphisms. Here, we report a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65340a60dc6cfcafb57dfef21fba0194
https://doi.org/10.1002/ajmg.a.37448