Your browser doesn't support javascript.
loading
Expansion of the clinical phenotype of the distal 10q26.3 deletion syndrome to include ataxia and hyperemia of the hands and feet.
Lacaria, Melanie; Srour, Myriam; Michaud, Jacques L; Doja, Asif; Miller, Elka; Schwartzentruber, Jeremy; Goldsmith, Claire; Majewski, Jacek; Boycott, Kym M.
Afiliação
  • Lacaria M; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario.
  • Srour M; Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec.
  • Michaud JL; Department of Pediatrics, McGill University, Montreal, Quebec.
  • Doja A; Research Center, Centre Hospitalier Universitaire Sainte-Justine, Montreal, Quebec.
  • Miller E; Department of Pediatrics, Universite de Montreal, Montreal, Quebec.
  • Schwartzentruber J; Department of Neurosciences, Universite de Montreal, Montreal, Quebec.
  • Goldsmith C; Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario.
  • Majewski J; Division of Neurology, Children's Hospital of Eastern Ontario, Ottawa, Ontario.
  • Boycott KM; Department of Medical Imaging, Children's Hospital of Eastern Ontario, Ottawa, Ontario.
Am J Med Genet A ; 173(6): 1611-1619, 2017 Jun.
Article em En | MEDLINE | ID: mdl-28432728
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ataxia / Deficiências do Desenvolvimento / Hiperemia / Deficiência Intelectual Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2017 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: Ataxia / Deficiências do Desenvolvimento / Hiperemia / Deficiência Intelectual Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article