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Publications by Lidia Larizza
Clinical Utility Gene Card For: Rothmund–Thomson Syndrome
European Journal of Human Genetics
Genetics
Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes
Frontiers in Genetics
Genetics
Molecular Medicine
Testing Single/Combined Clinical Categories on 5110 Italian Patients With Developmental Phenotypes to Improve Array-Based Detection Rate
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations
Frontiers in Pediatrics
Child Health
Pediatrics
Perinatology
High-Mobility Group A2 Gene Expression Is Frequently Induced in Non-Functioning Pituitary Adenomas (NFPAs), Even in the Absence of Chromosome 12 Polysomy
Endocrine-Related Cancer
Cancer Research
Endocrinology
Oncology
Metabolism
Diabetes
In VivoDifferentiation of Mast Cells From Acute Myeloid Leukemia Blasts Carrying a Novel Activating Ligand-Independent C-Kit Mutation
Blood Cells, Molecules, and Diseases
Molecular Medicine
Hematology
Molecular Biology
Cell Biology
Chronic Myelogenous Leukemia With Acquired C-Kit Activating Mutation and Transient Bone Marrow Mastocytosis
The Hematology Journal
