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Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2.
Guo, Tingwei; Diacou, Alexander; Nomaru, Hiroko; McDonald-McGinn, Donna M; Hestand, Matthew; Demaerel, Wolfram; Zhang, Liangtian; Zhao, Yingjie; Ujueta, Francisco; Shan, Jidong; Montagna, Cristina; Zheng, Deyou; Crowley, Terrence B; Kushan-Wells, Leila; Bearden, Carrie E; Kates, Wendy R; Gothelf, Doron; Schneider, Maude; Eliez, Stephan; Breckpot, Jeroen; Swillen, Ann; Vorstman, Jacob; Zackai, Elaine; Benavides Gonzalez, Felipe; Repetto, Gabriela M; Emanuel, Beverly S; Bassett, Anne S; Vermeesch, Joris R; Marshall, Christian R; Morrow, Bernice E.
Afiliación
  • Guo T; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Diacou A; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Nomaru H; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
  • McDonald-McGinn DM; Division of Human Genetics, Children's Hospital of Philadelphia and Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, USA.
  • Hestand M; Center for Human Genetics, Katholieke University Leuven (KULeuven), Leuven, Belgium.
  • Demaerel W; Center for Human Genetics, Katholieke University Leuven (KULeuven), Leuven, Belgium.
  • Zhang L; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Zhao Y; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Ujueta F; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Shan J; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Montagna C; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Zheng D; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Crowley TB; Department of Neurology, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Kushan-Wells L; Department of Neuroscience, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Bearden CE; Division of Human Genetics, Children's Hospital of Philadelphia and Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, USA.
  • Kates WR; Department of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, University of California at Los Angeles, Los Angeles, CA, USA.
  • Gothelf D; Department of Psychiatry and Biobehavioral Sciences, Semel Institute for Neuroscience and Human Behavior, University of California at Los Angeles, Los Angeles, CA, USA.
  • Schneider M; Department of Psychiatry and Behavioral Sciences, and Program in Neuroscience, SUNY Upstate Medical University, Syracuse, NY, USA.
  • Eliez S; Sackler Faculty of Medicine and Sagol School of Neuroscience, Tel Aviv University, Tel Aviv, Israel.
  • Breckpot J; Felsenstein Medical Research Center, Sackler Faculty of Medicine, Tel Aviv University, Petah Tikva, Israel.
  • Swillen A; Developmental Imaging and Psychopathology Lab, University of Geneva School of Medicine, Geneva, Switzerland.
  • Vorstman J; Developmental Imaging and Psychopathology Lab, University of Geneva School of Medicine, Geneva, Switzerland.
  • Zackai E; Center for Human Genetics, Katholieke University Leuven (KULeuven), Leuven, Belgium.
  • Benavides Gonzalez F; Center for Human Genetics, Katholieke University Leuven (KULeuven), Leuven, Belgium.
  • Repetto GM; Department of Psychiatry, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Emanuel BS; Division of Human Genetics, Children's Hospital of Philadelphia and Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, USA.
  • Bassett AS; Center for Genetics and Genomics, Facultad de Medicina, Clinica Alemana Universidad del Desarrollo, Santiago, Chile.
  • Vermeesch JR; Center for Genetics and Genomics, Facultad de Medicina, Clinica Alemana Universidad del Desarrollo, Santiago, Chile.
  • Marshall CR; Division of Human Genetics, Children's Hospital of Philadelphia and Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, USA.
  • Morrow BE; Center for Addiction and Mental Health, Toronto General Hospital and the University of Toronto, Toronto, Canada.
Hum Mol Genet ; 27(7): 1150-1163, 2018 04 01.
Article en En | MEDLINE | ID: mdl-29361080
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Mapeo Cromosómico / Síndrome de DiGeorge / Alelos / Meiosis Límite: Female / Humans / Male Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Mapeo Cromosómico / Síndrome de DiGeorge / Alelos / Meiosis Límite: Female / Humans / Male Idioma: En Revista: Hum Mol Genet Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos