Associated Papers
Rare variants modulating phenotype in NF1 carriers.
Pasquinelli E et al.
Scientific Reports, 2025
40653509 (PubMed )
Supplement: 41598_2025_9751_MOESM1_ESM.pdf
Is there a role for the IHH gene in Hirschsprung's disease?
Garcia-Barceló MM et al.
Neurogastroenterology and Motility, 2003
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