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Characterization of patients referred for non-specific intellectual disability testing: the importance of autosomal genes for diagnosis.
Tan, C A; Topper, S; Del Gaudio, D; Nelakuditi, V; Shchelochkov, O; Nowaczyk, M J M; Zeesman, S; Brady, L; Russell, L; Meeks, N; Sastry, S; Arndt, K; Kobiernicki, F; Shaw, R; Das, S.
Afiliação
  • Tan CA; Department of Human Genetics, University of Chicago, Chicago, IL, USA.
  • Topper S; Department of Human Genetics, University of Chicago, Chicago, IL, USA.
  • Del Gaudio D; Department of Human Genetics, University of Chicago, Chicago, IL, USA.
  • Nelakuditi V; Department of Human Genetics, University of Chicago, Chicago, IL, USA.
  • Shchelochkov O; Division of Genetics, University of Iowa Hospitals and Clinics, Iowa City, IA, USA.
  • Nowaczyk MJM; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.
  • Zeesman S; Department of Pediatrics, McMaster University, Hamilton, ON, Canada.
  • Brady L; Department of Pediatrics, McMaster University, Hamilton, ON, Canada.
  • Russell L; Department of Medical Genetics, Montreal General Hospital, Montreal, QC, Canada.
  • Meeks N; Department of Pediatrics, Section of Genetics, University of Colorado, Aurora, CO, USA.
  • Sastry S; Division of Genetic and Metabolic Disorders, Children's Hospital of Michigan, Detroit, MI, USA.
  • Arndt K; Department of Human Genetics, University of Chicago, Chicago, IL, USA.
  • Kobiernicki F; Department of Human Genetics, University of Chicago, Chicago, IL, USA.
  • Shaw R; Department of Human Genetics, University of Chicago, Chicago, IL, USA.
  • Das S; Department of Human Genetics, University of Chicago, Chicago, IL, USA.
Clin Genet ; 89(4): 478-483, 2016 Apr.
Article em En | MEDLINE | ID: mdl-25693842

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Clin Genet Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Clin Genet Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Estados Unidos