Your browser doesn't support javascript.
loading
6q22.1 microdeletion and susceptibility to pediatric epilepsy.
Szafranski, Przemyslaw; Von Allmen, Gretchen K; Graham, Brett H; Wilfong, Angus A; Kang, Sung-Hae L; Ferreira, Jose A; Upton, Sheila J; Moeschler, John B; Bi, Weimin; Rosenfeld, Jill A; Shaffer, Lisa G; Wai Cheung, Sau; Stankiewicz, Pawel; Lalani, Seema R.
Afiliação
  • Szafranski P; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Von Allmen GK; Division of Child and Adolescent Neurology, Department of Pediatrics, University of Texas Health Science Center at Houston, TX, USA.
  • Graham BH; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Wilfong AA; Department of Pediatric Neurology, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Kang SH; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Ferreira JA; Department of Pediatrics, University of South Florida, Tampa, FL, USA.
  • Upton SJ; Section of Medical Genetics, Department of Pediatrics, Dartmouth Hitchcock Medical Center, Lebanon, NH, USA.
  • Moeschler JB; Section of Medical Genetics, Department of Pediatrics, Dartmouth Hitchcock Medical Center, Lebanon, NH, USA.
  • Bi W; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Rosenfeld JA; Signature Genomic Laboratories, PerkinElmer Inc., Spokane, WA, USA.
  • Shaffer LG; Paw Print Genetics, Genetic Veterinary Sciences Inc., Spokane, WA, USA.
  • Wai Cheung S; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Stankiewicz P; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Lalani SR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Eur J Hum Genet ; 23(2): 173-9, 2015 Feb.
Article em En | MEDLINE | ID: mdl-24824130
Assuntos
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Membrana Transportadoras / Cromossomos Humanos Par 6 / Deleção de Genes / Epilepsia / Proteínas do Tecido Nervoso Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Membrana Transportadoras / Cromossomos Humanos Par 6 / Deleção de Genes / Epilepsia / Proteínas do Tecido Nervoso Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article