Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: a novel recognizable microdeletion syndrome?

Maria R osaria D'Apice, Antonio Novelli, Alessandra di Masi, Michela Biancolella, Antonio Antoccia, Francesca Gullotta, Norma Licata, Daniela Minella, Barbara Testa, Anna M aria Nardone, Giampiero Palmieri, Emma Calabrese, Livia Biancone, Caterina Tanzarella, Marina Frontali, Federica Sangiuolo, Giuseppe Novelli, Francesco Pallone

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Medicine & Life Sciences