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Whole exome sequencing of families with 1q21.1 microdeletion or microduplication.
Qiao, Ying; Badduke, Chansonette; Tang, Flamingo; Cowieson, David; Martell, Sally; Lewis, Suzanne M E; Peñaherrera, Maria S; Robinson, Wendy P; Volchuk, Allen; Rajcan-Separovic, Evica.
Afiliación
  • Qiao Y; Department of Pathology, University of British Columbia (UBC), Vancouver, British Columbia, Canada.
  • Badduke C; BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
  • Tang F; Department of Pathology, University of British Columbia (UBC), Vancouver, British Columbia, Canada.
  • Cowieson D; Department of Pathology, University of British Columbia (UBC), Vancouver, British Columbia, Canada.
  • Martell S; Division of Advanced Diagnostics-Metabolism Toronto General Research Institute, University Health Network, Toronto, Ontario, Canada.
  • Lewis SME; Department of Pathology, University of British Columbia (UBC), Vancouver, British Columbia, Canada.
  • Peñaherrera MS; BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
  • Robinson WP; Department of Medical Genetics, UBC, Vancouver, British Columbia, Canada.
  • Volchuk A; BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.
  • Rajcan-Separovic E; Department of Medical Genetics, UBC, Vancouver, British Columbia, Canada.
Am J Med Genet A ; 173(7): 1782-1791, 2017 Jul.
Article en En | MEDLINE | ID: mdl-28475290
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: Canadá
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2017 Tipo del documento: Article País de afiliación: Canadá