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

08:00 EDT 26th October 2017 | BioPortfolio

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

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Name: Genetics in medicine : official journal of the American College of Medical Genetics
ISSN: 1530-0366
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Medical and Biotech [MESH] Definitions

Federal program, enacted in 1997, for the funding of children's health insurance coverage at the state level for low-income families, affording them effective protection against erosions in employer sponsored coverage.

The type species of ERYTHROVIRUS and the etiological agent of ERYTHEMA INFECTIOSUM, a disease most commonly seen in school-age children.

A group of disorders characterized by an autosomal dominant pattern of inheritance with high rates of spontaneous mutation and multiple neurofibromas or neurilemmomas. NEUROFIBROMATOSIS 1 (generalized neurofibromatosis) accounts for approximately 95% of cases, although multiple additional subtypes (e.g., NEUROFIBROMATOSIS 2, neurofibromatosis 3, etc.) have been described. (From Neurochirurgie 1998 Nov;44(4):267-72)

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Pediatrics
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