<style face="normal" font="default" size="100%">Loss-of-function mutations in cause a new form of inherited thrombocytopenia.</style>

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<style face="normal" font="default" size="100%">Loss-of-function mutations in cause a new form of inherited thrombocytopenia.</style>

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<style face="normal" font="default" size="100%">MYH9-Related Thrombocytopenia: Four Novel Variants Affecting the Tail Domain of the Non-Muscle Myosin Heavy Chain IIA Associated with a Mild Clinical Evolution of the Disorder.</style>

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<style face="normal" font="default" size="100%">ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia.</style>

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<style face="normal" font="default" size="100%">Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia.</style>

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<style face="normal" font="default" size="100%">MYH9: Structure, functions and role of non-muscle myosin IIA in human disease.</style>

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<style face="normal" font="default" size="100%">A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin gene.</style>

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<style face="normal" font="default" size="100%">Gray platelet syndrome: Novel mutations of the NBEAL2 gene.</style>

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<style face="normal" font="default" size="100%">Mutations of RUNX1 in families with inherited thrombocytopenia.</style>

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<style face="normal" font="default" size="100%">MYH9 gene mutations associated with bleeding.</style>

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<style face="normal" font="default" size="100%">Clinical and pathogenetic features of ETV6 related thrombocytopenia with predisposition to acute lymphoblastic leukemia.</style>

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<style face="normal" font="default" size="100%">Evaluation of energy metabolism and calcium homeostasis in cells affected by Shwachman-Diamond syndrome.</style>

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<style face="normal" font="default" size="100%">Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related Disease.</style>

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<style face="normal" font="default" size="100%">Somatic, hematologic phenotype, long-term outcome, and effect of hematopoietic stem cell transplantation. An analysis of 97 Fanconi anemia patients from the Italian national database on behalf of the Marrow Failure Study Group of the AIEOP (Italian Associ</style>

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<style face="normal" font="default" size="100%">Abnormal cytoplasmic extensions associated with active αIIbβ3 are probably the cause for macrothrombocytopenia in Glanzmann thrombasthenia-like syndrome.</style>

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<style face="normal" font="default" size="100%">ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization.</style>

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<style face="normal" font="default" size="100%">Clinical aspects of Fanconi anemia individuals with the same mutation of FANCF identified by next generation sequencing.</style>

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<style face="normal" font="default" size="100%">Germline mutations in ETV6 are associated with thrombocytopenia, red cell macrocytosis and predisposition to lymphoblastic leukemia.</style>

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<style face="normal" font="default" size="100%">Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia.</style>

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<style face="normal" font="default" size="100%">Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology.</style>

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<style face="normal" font="default" size="100%">Mutations of cytochrome c identified in patients with thrombocytopenia THC4 affect both apoptosis and cellular bioenergetics.</style>

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<style face="normal" font="default" size="100%">MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations.</style>

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<style face="normal" font="default" size="100%">Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders.</style>

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<style face="normal" font="default" size="100%">Polyubiquitinated proteins, proteasome, and glycogen characterize the particle-rich cytoplasmic structure (PaCS) of neoplastic and fetal cells.</style>

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<style face="normal" font="default" size="100%">Spectrum of the mutations in Bernard-Soulier syndrome.</style>

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<style face="normal" font="default" size="100%">Unusual splice site mutations disrupt FANCA exon 8 definition.</style>

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<style face="normal" font="default" size="100%">MYH9-related disease: five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations.</style>

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<style face="normal" font="default" size="100%">Alteration of liver enzymes is a feature of the MYH9-related disease syndrome.</style>

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<style face="normal" font="default" size="100%">Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation).</style>

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<style face="normal" font="default" size="100%">MYH9-related disorders: report on a patient of Greek origin presenting with macroscopic hematuria and presenile cataract, caused by an R1165C mutation.</style>

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<style face="normal" font="default" size="100%">Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlations.</style>

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<style face="normal" font="default" size="100%">Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families.</style>

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<style face="normal" font="default" size="100%">Mutations in the 5' UTR of ANKRD26, the ankirin repeat domain 26 gene, cause an autosomal-dominant form of inherited thrombocytopenia, THC2.</style>

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<style face="normal" font="default" size="100%">Recent advances in the understanding and management of MYH9-related inherited thrombocytopenias.</style>

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<style face="normal" font="default" size="100%">Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations.</style>

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<style face="normal" font="default" size="100%">Expression and association data strongly support JARID2 involvement in nonsyndromic cleft lip with or without cleft palate.</style>

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<style face="normal" font="default" size="100%">A G to C transversion at the last nucleotide of exon 25 of the MYH9 gene results in a missense mutation rather than in a splicing defect.</style>

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<style face="normal" font="default" size="100%">MYH9-related disease: Report on five German families and description of a novel mutation.</style>