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Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age.
Brownstein, Catherine A; Douard, Elise; Haynes, Robin L; Koh, Hyun Yong; Haghighi, Alireza; Keywan, Christine; Martin, Bree; Alexandrescu, Sanda; Haas, Elisabeth A; Vargas, Sara O; Wojcik, Monica H; Jacquemont, Sébastien; Poduri, Annapurna H; Goldstein, Richard D; Holm, Ingrid A.
Afiliação
  • Brownstein CA; Robert's Program on Sudden Unexplained Death in Pediatrics Boston Children's Hospital Boston MA 02115 USA.
  • Douard E; Division of Genetics and Genomics Boston Children's Hospital Boston MA 02115 USA.
  • Haynes RL; The Manton Center for Orphan Disease Research Boston Children's Hospital Boston MA 02115 USA.
  • Koh HY; Department of Pediatrics Harvard Medical School Boston MA 02115 USA.
  • Haghighi A; Sainte Justine Hospital Research Center Montreal Quebec H3T 1C5 Canada.
  • Keywan C; Department of Neuroscience University of Montreal Montreal Quebec H3C 3J7 Canada.
  • Martin B; Robert's Program on Sudden Unexplained Death in Pediatrics Boston Children's Hospital Boston MA 02115 USA.
  • Alexandrescu S; Department of Pathology Boston Children's Hospital and Harvard Medical School Boston MA 02115 USA.
  • Haas EA; Robert's Program on Sudden Unexplained Death in Pediatrics Boston Children's Hospital Boston MA 02115 USA.
  • Vargas SO; Division of Genetics and Genomics Boston Children's Hospital Boston MA 02115 USA.
  • Wojcik MH; The Manton Center for Orphan Disease Research Boston Children's Hospital Boston MA 02115 USA.
  • Jacquemont S; Epilepsy Genetics Program Department of Neurology Boston Children's Hospital Boston MA 02115 USA.
  • Poduri AH; F. M. Kirby Neurobiology Center Department of Neurology Boston Children's Hospital Boston MA 02115 USA.
  • Goldstein RD; Department of Neurology Harvard Medical School Boston MA 02115 USA.
  • Holm IA; Department of Genetics Harvard Medical School Boston MA 02115 USA.
Adv Genet (Hoboken) ; 4(1): 2200012, 2023 Mar.
Article em En | MEDLINE | ID: mdl-36910592
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies Idioma: En Revista: Adv Genet (Hoboken) Ano de publicação: 2023 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Guideline / Prognostic_studies Idioma: En Revista: Adv Genet (Hoboken) Ano de publicação: 2023 Tipo de documento: Article