• 8966 Citations
  • 49 h-Index
1989 …2019
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Fingerprint Dive into the research topics where Maria Cristina Digilio is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

Medicine & Life Sciences

Congenital Heart Defects
DiGeorge Syndrome
Mutation
Noonan Syndrome
Genes
Phenotype
LEOPARD Syndrome
Down Syndrome
Intellectual Disability
Tetralogy of Fallot
Heart Diseases
Hypertrophic Cardiomyopathy
Williams Syndrome
Chromosomes
Genetic Association Studies
Haploinsufficiency
Ellis-Van Creveld Syndrome
Missense Mutation
Costello Syndrome
Thoracic Aorta
Pulmonary Valve Stenosis
Germ-Line Mutation
Microcephaly
Growth
Transposition of Great Vessels
Chromosome Deletion
Mothers
Aortic Coarctation
Lentigo
Ventricular Heart Septal Defects
Siblings
Exons
Neurofibromatosis 1
Cardiovascular Abnormalities
Newborn Infant
CHARGE Syndrome
Recurrence
Neurofibromatosis 1 Genes
Single Nucleotide Polymorphism
Heterotaxy Syndrome
Atrial Heart Septal Defects
Karyotype
Italy
Truncus Arteriosus
Kidney
Fluorescence In Situ Hybridization
Celiac Disease
Mitral Valve
Inborn Genetic Diseases
Exome