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Hypermobile Ehlers-Danlos syndrome (hEDS) phenotype in fragile X premutation carriers: case series.
Tassanakijpanich, Nattaporn; McKenzie, Forrest J; McLennan, Yingratana A; Makhoul, Elisabeth; Tassone, Flora; Jasoliya, Mittal J; Romney, Christopher; Petrasic, Ignacio Cortina; Napalinga, Kaye; Buchanan, Caroline B; Hagerman, Paul; Hagerman, Randi; Casanova, Emily L.
Afiliação
  • Tassanakijpanich N; Department of Pediatrics, Faculty of Medicine, Prince of Songkla University, Hat Yai, Thailand.
  • McKenzie FJ; UC Davis MIND Institute, UC Davis Health, Sacramento, California, USA.
  • McLennan YA; UC Davis MIND Institute, UC Davis Health, Sacramento, California, USA.
  • Makhoul E; University of California, Davis, School of Medicine, Sacramento, California, USA.
  • Tassone F; UC Davis MIND Institute, UC Davis Health, Sacramento, California, USA.
  • Jasoliya MJ; Department of Pediatrics, University of California, Davis, School of Medicine, Sacramento, California, USA.
  • Romney C; UC Davis MIND Institute, UC Davis Health, Sacramento, California, USA.
  • Petrasic IC; Department of Biochemistry and Molecular Medicine, University of California, Davis, School of Medicine, Sacramento, California, USA.
  • Napalinga K; UC Davis MIND Institute, UC Davis Health, Sacramento, California, USA.
  • Buchanan CB; Department of Biochemistry and Molecular Medicine, University of California, Davis, School of Medicine, Sacramento, California, USA.
  • Hagerman P; Department of Biochemistry and Molecular Medicine, University of California, Davis, School of Medicine, Sacramento, California, USA.
  • Hagerman R; UC Davis MIND Institute, UC Davis Health, Sacramento, California, USA.
  • Casanova EL; UC Davis MIND Institute, UC Davis Health, Sacramento, California, USA.
J Med Genet ; 59(7): 687-690, 2022 07.
Article em En | MEDLINE | ID: mdl-34193467
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Ehlers-Danlos / Síndrome do Cromossomo X Frágil Tipo de estudo: Diagnostic_studies Limite: Child, preschool / Female / Humans / Male Idioma: En Revista: J Med Genet Ano de publicação: 2022 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: Síndrome de Ehlers-Danlos / Síndrome do Cromossomo X Frágil Tipo de estudo: Diagnostic_studies Limite: Child, preschool / Female / Humans / Male Idioma: En Revista: J Med Genet Ano de publicação: 2022 Tipo de documento: Article