No abstract available
MeSH terms
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22q11 Deletion Syndrome / diagnosis*
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22q11 Deletion Syndrome / genetics
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22q11 Deletion Syndrome / pathology
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Biomarkers / analysis
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Female
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Heart Defects, Congenital / diagnosis*
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Heart Defects, Congenital / genetics
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Heart Defects, Congenital / pathology
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Humans
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In Situ Hybridization, Fluorescence
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Infant
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Karyotyping
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Male
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Predictive Value of Tests
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Prospective Studies
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ROC Curve
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Thrombocytopenia / diagnosis*
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Thrombocytopenia / genetics
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Thrombocytopenia / pathology