Associated Papers
A new variant of MYCN gene as a cause of Feingold syndrome.
Zeka N et al.
Clinical Case Reports, 2022
Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia.
Cognet M et al.
European Journal of Human Genetics : Ejhg, 2011
Genotype-phenotype correlations in MYCN-related Feingold syndrome.
Marcelis CL et al.
Human Mutation, 2008
Select a paper to view details