Condition: FEINGOLD SYNDROME 1
rs104893646
in
MYCN
gene and
FEINGOLD SYNDROME 1
PMID 18470948
2008 Genotype-phenotype correlations in MYCN-related Feingold syndrome.
PMID 15821734
2005 MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndrome.
PMID 16906565
2006 Expanding the clinical spectrum of MYCN-related Feingold syndrome.