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A New Case of Rare Microdeletion 10q22.3q23 along with Mosaic Klinefelter Syndrome Associated with Facial Dysmorphic Finding, Atrial Ventricular Septal Defect, and Motor Retardation
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O. Ozdemır
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F. Sılan
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Jelena Veličković
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Firdevs Dinçsoy Bir
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Mehmet Berkay Akcan
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