School liaison program supporting children with neurofibromatosis type 1: a model of care for children with chronic disease

Genet Med. 2018 Jul;20(7):785-788. doi: 10.1038/gim.2017.177. Epub 2017 Oct 26.

Authors

Meredith A Chambers¹, David T Miller², Nicole J Ullrich³

Affiliations

¹ Department of Neurology, Boston Children's Hospital, Boston, Massachusetts, USA.
² Department of Medicine/Division of Genetics and Genomics, Boston Children's Hospital, Boston, Massachusetts, USA.
³ Department of Neurology, Boston Children's Hospital, Boston, Massachusetts, USA. nicole.ullrich@childrens.harvard.edu.

PMID: 29261174
DOI: 10.1038/gim.2017.177

No abstract available

Publication types

Editorial

MeSH terms

Child
Child, Preschool
Chronic Disease
Education of Intellectually Disabled / methods*
Female
Humans
Male
Models, Educational
Neurofibromatosis 1 / therapy*
School Health Services / standards*