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Approaches to studying the impact of 22q11.2 copy number variants.
Bassett, Anne S; McDonald-McGinn, Donna M; Boot, Erik; Óskarsdóttir, Sólveig; Yuen, Ryan K C.
Afiliación
  • Bassett AS; The Dalglish Family 22q Clinic for Adults, and Department of Psychiatry, University Health Network, Toronto, ON, Canada; Toronto General Research Institute and Division of Cardiology, Department of Medicine, University Health Network, Toronto, ON, Canada; Clinical Genetics Research Program and Campb
  • McDonald-McGinn DM; 22q and You Center, Clinical Genetics Center, and Section of Genetic Counseling, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA; Department of Pediatrics, Perelman School of Medicine of the University of Pennsylvania, Philadelphia, PA, USA; Department of Human
  • Boot E; The Dalglish Family 22q Clinic for Adults, and Department of Psychiatry, University Health Network, Toronto, ON, Canada; Advisium, 's Heeren Loo Zorggroep, Amersfoort, the Netherlands; Department of Psychiatry and Neuropsychology, Maastricht University, Maastricht, the Netherlands.
  • Óskarsdóttir S; Department of Pediatric Rheumatology and Immunology, Queen Silvia Children's Hospital, SahlgrenskaUniversity Hospital, Gothenburg, Sweden; Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
  • Yuen RKC; Genetics & Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada; Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada.
Am J Hum Genet ; 110(7): 1216-1218, 2023 07 06.
Article en En | MEDLINE | ID: mdl-37419092
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de DiGeorge / Variaciones en el Número de Copia de ADN Límite: Humans Idioma: En Revista: Am J Hum Genet Año: 2023 Tipo del documento: Article
Texto completo
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XML
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de DiGeorge / Variaciones en el Número de Copia de ADN Límite: Humans Idioma: En Revista: Am J Hum Genet Año: 2023 Tipo del documento: Article