Palate abnormalities in Chilean patients with chromosome 22q11 microdeletion syndrome

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Journal Title

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Publisher

Elsevier

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3

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Abstract

OBJECTIVE: Chromosome 22q11 microdeletion syndrome (del22q11) is the most frequent microdeletion syndrome in humans, with an estimated incidence of 1/4000. It is recognized as a common identifiable c...

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Centro de Genética y Genómica

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Citation

International Journal Pediatrics Otorhinolaryngology, 2012, 76(12):1726-8

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