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Clinical exome sequencing uncovers a high frequency of Mendelian disorders in infants with stroke: A retrospective analysis.
Kumar, Runjun D; Meng, Linyan; Liu, Pengfei; Miyake, Christina Y; Worley, Kim C; Bi, Weimin; Lalani, Seema R.
  • Kumar RD; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Meng L; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Liu P; Baylor Genetics Laboratories, Houston, Texas, USA.
  • Miyake CY; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Worley KC; Baylor Genetics Laboratories, Houston, Texas, USA.
  • Bi W; Department of Pediatrics, Division of Cardiology, Baylor College of Medicine, Houston, Texas, USA.
  • Lalani SR; Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, Texas, USA.
Am J Med Genet A ; 188(11): 3184-3190, 2022 11.
Article en En | MEDLINE | ID: mdl-36065636
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Accidente Cerebrovascular / Exoma Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Accidente Cerebrovascular / Exoma Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article