<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%">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%">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%">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%">Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia.</style>