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Diagnosis of 22q11.2 Deletion Syndrome in a Child With Congenital Heart Disease and Facial Dimorphism: A Case Report
by
Moura Carvalho, Natalia Dayane
,
Camargo, Ronaldo Castillo
,
Costa Garcia, Heliana Maria
,
Silva Teles, Suely Regina da
,
Fantin, Cleiton
Published in
Acta medica Iranica
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Acta Medica Iranica
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Cardiovascular Disease
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Chromosome 22
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Congenital Diseases
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Fluorescence In Situ Hybridization
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Fluorescence In Situ Hybridizations
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Genetic Counseling
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Region 22Q11.2
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Region N25
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