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Now showing items 1-9 of 9
A Nationwide Registry-Based Study on Mortality Due to Rare Congenital Anomalies
Analysis of Mortality among Neonates and Children with Spina Bifida: An International Registry-Based Study, 2001-2012.
Expanding the genotypic and phenotypic spectrum of severe serine biosynthesis disorders.
Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum
Prevention of Neural Tube Defects in Europe: A Public Health Failure.
Primary prevention as an essential factor ensuring sustainability of health systems: the example of congenital anomalies.
SpainUDP: The Spanish Undiagnosed Rare Diseases Program
Tetralogy of Fallot in Spain: a nationwide registry-based mortality study across 36 years