Associated Papers
Atypical Melanocytic Matricoma: A Case Report with Molecular Studies.
Feoli F et al.
The American Journal of Dermatopathology, 2023
A Novel MYCN Variant Associated with Intellectual Disability Regulates Neuronal Development.
Yu X et al.
Neuroscience Bulletin, 2018
Feingold syndrome associated with two novel MYCN mutations in sporadic and familial cases including monozygotic twins.
Blaumeiser B et al.
American Journal of Medical Genetics. Part A, 2008
Genotype-phenotype correlations in MYCN-related Feingold syndrome.
Marcelis CL et al.
Human Mutation, 2008
Feingold syndome: a rare but important cause of syndromic tracheoesophageal fistula.
Layman-Pleet L et al.
Journal of Pediatric Surgery, 2007
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