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Pure 21q22.3 deletion identified in a patient with mild phenotypic features.
Ilária Cristina Sgardioli
Matheus de Melo Copelli
Elaine Lustosa-Mendes
Társis Paiva Vieira
Vera Lúcia Gil-da-Silva-Lopes
Published in:
Congenital anomalies (2018)
Keyphrases
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case report