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Publications by Eti A. Femia
P2Y12 Receptor Gene Mutations Associated With Bleeding
Platelets
Medicine
Hematology
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Haploinsufficiency of the Platelet P2Y12 Gene in a Family With Congenital Bleeding Diathesis.
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Haploinsufficiency of the Platelet P2Y12 Gene in a Family With Congenital Bleeding Diathesis
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Hyperinsulinemic Hypoglycemia Syndrome Associated With Mutations in the Human Insulin Receptor Gene: Report of Two Cases
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ITGA2B and ITGB3 Gene Mutations Associated With Glanzmann Thrombasthenia
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Platelet Membrane Receptor P2Y12 H1/H2 Polymorphisms Is Highly Associated With Cerebral Infarction: A Case-Control Study
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Cardiomyopathies Associated With the DES Gene Mutations: Molecular Pathogenesis and Gene Therapy Approaches
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Gonadal Function in 15 Patients Associated With WT1 Gene Mutations
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Mutations in the Nebulin Gene Associated With Autosomal Recessive Nemaline Myopathy
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Multidisciplinary