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Publications by Marco Tartaglia
Corrigendum: Gain-Of-Function SOS1 Mutations Cause a Distinctive Form of Noonan Syndrome
Nature Genetics
Genetics
PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity
American Journal of Human Genetics
Genetics
NF1 Gene Mutations Represent the Major Molecular Event Underlying Neurofibromatosis-Noonan Syndrome
American Journal of Human Genetics
Genetics
Acute Lymphoblastic Leukemia-Associated JAK1 Mutants Activate the Janus Kinase/Stat Pathway via Interleukin-9 Receptor Α Homodimers
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Decreased Proliferation and Altered Differentiation in Osteoblasts From Genetically and Clinically Distinct Craniosynostotic Disorders
American Journal of Pathology
Forensic Medicine
Pathology
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