• 10246 Citations
  • 47 h-Index
1990 …2019
If you made any changes in Pure these will be visible here soon.

Fingerprint Dive into the research topics where Marco Tartaglia is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

Medicine & Life Sciences

Mutation
Noonan Syndrome
Phenotype
Exome
Genes
Missense Mutation
LEOPARD Syndrome
Costello Syndrome
Germ-Line Mutation
Intellectual Disability
Hypertrophic Cardiomyopathy
Congenital Heart Defects
Growth
Proteins
Neoplasms
Genetic Association Studies
Non-Receptor Type 11 Protein Tyrosine Phosphatase
Ataxia
Juvenile Myelomonocytic Leukemia
Brain Diseases
Saposins
Protein Tyrosine Phosphatases
Mitogen-Activated Protein Kinases
Craniosynostoses
Cofilin 2
Exons
Neoplastic Stem Cells
Codon
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Inborn Genetic Diseases
Alleles
Phosphoric Monoester Hydrolases
Transducers
Signal Transduction
Amino Acid Substitution
Ellis-Van Creveld Syndrome
Pediatrics
SH2 Domain-Containing Protein Tyrosine Phosphatases
Mutant Proteins
Colorectal Neoplasms
Phosphotransferases
Microcephaly
Myotonia Congenita
src Homology Domains