Prenatal Diagnosis by Trio Clinical Exome Sequencing: Single Center Experience von Margiotti, Katia, Fabiani, Marco, Cima, Antonella, Libotte, Francesco, Mesoraca, Alvaro, Giorlandino, Claudio

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Digenic Origin of Difference of Sex Development in a Patient Harbouring DHX37 and MAMLD1 Variants von Margiotti, Katia, Libotte, Francesco, Fabiani, Marco, Mesoraca, Alvaro, Giorlandino, Claudio

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Pallister–Killian syndrome: Cytogenetics and molecular investigations of mosaic tetrasomy 12p in prenatal chorionic villus and in amniocytes. Strategy of prenatal diagnosis von Libotte, Francesco, Bizzoco, Domenico, Gabrielli, Ivan, Mesoraca, Alvaro, Cignini, Pietro, Vitale, Salvatore Giovanni, Marilli, Ilaria, Gulino, Ferdinando Antonio, Rapisarda, Agnese Maria Chiara, Giorlandino, Claudio

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De novo 3q13.13q21.2 interstitial deletion and paternal 12p13.3 microdeletion in a fetus with dysplasia of the corpus callosum and ventriculomegaly: A case report von Libotte, Francesco, Fabiani, Marco, Margiotti, Katia, Carpineto, Lorena Sonia, Monaco, Francesca, Raffio, Raffaella, Mesoraca, Alvaro, Giorlandino, Claudio

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Prenatal Diagnosis of Combined Maternal 4q Interstitial Deletion and Paternal 15q Microduplication von Libotte, Francesco, Fabiani, Marco, Margiotti, Katia, Viola, Antonella, Mesoraca, Alvaro, Giorlandino, Claudio

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Agnathia-Otocephaly Complex Due to a De Novo Deletion in the IOTX2/I Gene von Fabiani, Marco, Libotte, Francesco, Margiotti, Katia, Tannous, Dina Khader Issa, Sparacino, Davide, D’Aleo, Maria Pia, Monaco, Francesca, Dello Russo, Claudio, Mesoraca, Alvaro, Giorlandino, Claudio

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Agnathia-Otocephaly Complex Due to a De Novo Deletion in the OTX2 Gene von Fabiani, Marco, Libotte, Francesco, Margiotti, Katia, Tannous, Dina Khader Issa, Sparacino, Davide, D'Aleo, Maria Pia, Monaco, Francesca, Dello Russo, Claudio, Mesoraca, Alvaro, Giorlandino, Claudio

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Cytogenetics and Molecular Investigations detect a Mosaic Variant of Turner Syndrome only Suspected by Non-Invasive Prenatal Testing: Two Case Reports with Negative Ultrasound Exam... von Libotte, Francesco, Carpineto, Sonia Lorena, Dello Russo, Claudio, Viola, Antonella, Margiotti, Katia, Restaldi, Fabrizia, Novelli, Antonio, Mesoraca, Alvaro, Giorlandino, Claudio

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A new case of interstitial 1q 25.3-32.1 deletion: cytogenetic analysis molecular characterization and ultrasound findings von Libotte, Francesco, Bizzoco, Domenico, Gabrielli, Ivan, Tamburrino, Caterina, Ernandez, Cristina, Carpineto, Lorena, D'Aleo, Maria Pia, Cima, Antonella, Mesoraca, Alvaro, Cignini, Pietro, Aloisi, Alessia, Angioli, Roberto, Vitale, Salvatore Giovanni, Giorlandino, Claudio

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BCL-2/BCL-XL Inhibition in Smoldering Multiple Myeloma CD138+ Cells: Functional Effects and Protein Expression Levels von Libotte, Francesco, Ricciardi, Maria Rosaria, Calabrese, Elisabetta, De Benedictis, Cinzia, Santinelli, Sara, Bergamo, Paola, Decandia, Samantha, Levi, Anna, Mohamad, Ali Fathi, Federico, Vincenzo, Milella, Michele, Foà, Robert, Tafuri, Agostino, Petrucci, Maria Teresa

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Multiple Strategies Based on MEK, mTOR and BCL-2 Signal Transduction Inhibition in Acute Lymphoblastic Leukemia (ALL) von Ricciardi, Maria Rosaria, Decandia, Samantha, Santinelli, Sara, Gregorj, Chiara, De Cave, Fabiana, Scerpa, Maria Cristina, Bergamo, Paola, Libotte, Francesco, De Benedictis, Cinzia, Vitale, Antonella, Petrucci, Maria Teresa, Konopleva, Marina, Andreeff, Michael, Milella, Michele, Foa, Robert, Tafuri, Agostino

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Synergistic Induction of Apoptosis in Multiple Myeloma Cells by Simultaneous Inhibition of the Raf/MEK/ERK and BCL-2 Pathways von Ricciardi, Maria Rosaria, Milella, Michele, Libotte, Francesco, Calabrese, Elisabetta, Bergamo, Paola, Santinelli, Sara, Decandia, Samantha, De Benedictis, Cinzia, Levi, Anna, Foà, Robert, Tafuri, Agostino, Petrucci, Maria Teresa

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Development of Mek inhibition (MEK-I)-Based Therapeutic Strategies in Acute Myeloid Leukemia (AML) von Milella, Michele, Ricciardi, Maria Rosaria, Bergamo, Paola, Scerpa, Maria Cristina, Gervasoni, Jacopo, Petrucci, Maria Teresa, Chiaretti, Sabina, Tavolaro, Simona, Ciuffreda, Ludovica, Decandia, Samantha, Libotte, Francesco, Abrams, Stephen Lee, Steelman, Linda S, Konopleva, Marina, Cognetti, Francesco, Foa, Robert, Andreeff, Michael, McCubrey, James, Tafuri, Agostino

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Prenatal Diagnosis of Combined Maternal 4q Interstitial Deletion and Paternal 15q Microduplication von Libotte, Francesco, Fabiani, Marco, Margiotti, Katia, Viola, Antonella, Mesoraca, Alvaro, Giorlandino, Claudio

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A new case of interstitial 1q 25.3-32.1 deletion: cytogenetic analysis molecular characterization and ultrasound findings von Libotte, Francesco, Bizzoco, Domenico, Gabrielli, Ivan, Tamburrino, Caterina, Ernandez, Cristina, Carpineto, Lorena, D'Aleo, Maria Pia, Cima, Antonella, Mesoraca, Alvaro, Cignini, Pietro, Aloisi, Alessia, Angioli, Roberto, Vitale, Salvatore Giovanni, Giorlandino, Claudio

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