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.