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Refining the Phenotype of Recurrent Rearrangements of Chromosome 16.
Redaelli, Serena; Maitz, Silvia; Crosti, Francesca; Sala, Elena; Villa, Nicoletta; Spaccini, Luigina; Selicorni, Angelo; Rigoldi, Miriam; Conconi, Donatella; Dalprà, Leda; Roversi, Gaia; Bentivegna, Angela.
Affiliation
  • Redaelli S; School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy. serena.redaelli@unimib.it.
  • Maitz S; Clinical Pediatric Genetics Unit, Pediatrics Clinics, MBBM Foundation, S. Gerardo Hospital, 20900 Monza, Italy. maitz.silvia@gmail.com.
  • Crosti F; Medical Genetics Laboratory, Clinical Pathology Department, S. Gerardo Hospital, 20900 Monza, Italy. f.crosti@asst-monza.it.
  • Sala E; Medical Genetics Laboratory, Clinical Pathology Department, S. Gerardo Hospital, 20900 Monza, Italy. elena.sala@asst-monza.it.
  • Villa N; Medical Genetics Laboratory, Clinical Pathology Department, S. Gerardo Hospital, 20900 Monza, Italy. n.villa@asst-monza.it.
  • Spaccini L; Clinical Genetics Unit, Department of Obstetrics and Gynecology, V. Buzzi Children's Hospital, University of Milan, 20154 Milan, Italy. luigina.spaccini@asst-fbf-sacco.it.
  • Selicorni A; Clinical Pediatric Unit, ASST Lariana, 22042 Como, Italy. angelo.selicorni61@gmail.com.
  • Rigoldi M; Medical Genetics Laboratory, Clinical Pathology Department, S. Gerardo Hospital, 20900 Monza, Italy. rigoldimiriam@gmail.com.
  • Conconi D; School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy. donatella.conconi@unimib.it.
  • Dalprà L; School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy. leda.dalpra@unimib.it.
  • Roversi G; School of Medicine and Surgery, University of Milano-Bicocca, 20900 Monza, Italy. gaia.roversi@unimib.it.
  • Bentivegna A; Medical Genetics Laboratory, Clinical Pathology Department, S. Gerardo Hospital, 20900 Monza, Italy. gaia.roversi@unimib.it.
Int J Mol Sci ; 20(5)2019 Mar 04.
Article in En | MEDLINE | ID: mdl-30836598
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Full text: 1 Database: MEDLINE Main subject: Abnormalities, Multiple / Chromosomes, Human, Pair 16 / Developmental Disabilities / Comparative Genomic Hybridization Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Language: En Journal: Int J Mol Sci Year: 2019 Type: Article Affiliation country: Italy
Fulltext
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Full text: 1 Database: MEDLINE Main subject: Abnormalities, Multiple / Chromosomes, Human, Pair 16 / Developmental Disabilities / Comparative Genomic Hybridization Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Language: En Journal: Int J Mol Sci Year: 2019 Type: Article Affiliation country: Italy