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Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins.
Vervoort, Lisanne; Demaerel, Wolfram; Rengifo, Laura Y; Odrzywolski, Adrian; Vergaelen, Elfi; Hestand, Matthew S; Breckpot, Jeroen; Devriendt, Koen; Swillen, Ann; McDonald-McGinn, Donna M; Fiksinski, Ania M; Zinkstok, Janneke R; Morrow, Bernice E; Heung, Tracy; Vorstman, Jacob A S; Bassett, Anne S; Chow, Eva W C; Shashi, Vandana; Vermeesch, Joris R.
Afiliação
  • Vervoort L; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Demaerel W; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Rengifo LY; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Odrzywolski A; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Vergaelen E; Department of Biochemistry and Molecular Biology, Medical University of Lublin, Lublin, Poland.
  • Hestand MS; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Breckpot J; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Devriendt K; Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Swillen A; Department of Pediatrics, University of Cincinnati, Cincinnati, OH, USA.
  • McDonald-McGinn DM; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Fiksinski AM; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Zinkstok JR; Department of Human Genetics, KU Leuven, Leuven, Belgium.
  • Morrow BE; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Heung T; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Vorstman JAS; Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Bassett AS; The Dalglish Family 22q Clinic and Centre for Addiction and Mental Health, Toronto, ON, Canada.
  • Chow EWC; Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Shashi V; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
  • Vermeesch JR; Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht, The Netherlands.
Hum Mol Genet ; 28(22): 3724-3733, 2019 11 15.
Article em En | MEDLINE | ID: mdl-31884517
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de DiGeorge / Recombinação Homóloga Limite: Adult / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de DiGeorge / Recombinação Homóloga Limite: Adult / Female / Humans / Male Idioma: En Ano de publicação: 2019 Tipo de documento: Article